Imported Disease Annotations - OMIM |
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Imported Disease Annotations - OMIM |
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# | Reference Title | Reference Citation |
1. | OMIM Disease Annotation Pipeline | OMIM Disease Annotation Pipeline |
2. | ClinVar Automated Import and Annotation Pipeline | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
3. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
4. | RGD HPO Phenotype Annotation Pipeline | RGD automated import pipeline for human HPO-to-gene-to-disease annotations |
PMID:11347906 | PMID:12477932 | PMID:12714037 | PMID:12766169 | PMID:14702039 | PMID:15922909 | PMID:18391951 | PMID:18978678 | PMID:20379614 | PMID:21873635 | PMID:22889924 | PMID:22898364 |
PMID:23192621 | PMID:24564958 | PMID:24986830 | PMID:26235311 | PMID:28276056 | PMID:28322503 | PMID:28344315 | PMID:29150431 | PMID:30359423 | PMID:31343991 | PMID:31482140 | PMID:31903681 |
PMID:32360765 | PMID:32376988 | PMID:33359165 | PMID:33536335 | PMID:34299191 |
COL27A1 (Homo sapiens - human) |
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Col27a1 (Mus musculus - house mouse) |
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Col27a1 (Rattus norvegicus - Norway rat) |
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Col27a1 (Chinchilla lanigera - long-tailed chinchilla) |
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COL27A1 (Pan paniscus - bonobo/pygmy chimpanzee) |
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COL27A1 (Canis lupus familiaris - dog) |
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Col27a1 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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COL27A1 (Sus scrofa - pig) |
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COL27A1 (Chlorocebus sabaeus - green monkey) |
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Col27a1 (Heterocephalus glaber - naked mole-rat) |
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Variants in COL27A1
2043 total Variants |
Name | Type | Condition(s) | Position(s) | Clinical significance |
NM_032888.4(COL27A1):c.594C>T (p.Leu198=) | single nucleotide variant | not provided [RCV001494525] | Chr9:114168149 [GRCh38] Chr9:116930429 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2089G>C (p.Gly697Arg) | single nucleotide variant | Steel syndrome [RCV000132771]|not provided [RCV000337500] | Chr9:114195977 [GRCh38] Chr9:116958257 [GRCh37] Chr9:9q32 |
pathogenic |
GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1 | copy number loss | See cases [RCV000050315] | Chr9:99138048..115011033 [GRCh38] Chr9:101900330..117773312 [GRCh37] Chr9:100940151..116813133 [NCBI36] Chr9:9q22.33-33.1 |
pathogenic |
NM_032888.4(COL27A1):c.1891_1908+1dup | duplication | not provided [RCV001246854] | Chr9:114169444..114169445 [GRCh38] Chr9:116931724..116931725 [GRCh37] Chr9:9q32 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 | copy number gain | See cases [RCV000050348] | Chr9:193412..138179445 [GRCh38] Chr9:204193..141073897 [GRCh37] Chr9:194193..140193718 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9q32(chr9:114246876-114637081)x3 | copy number gain | See cases [RCV000052236] | Chr9:114246876..114637081 [GRCh38] Chr9:117009156..117399361 [GRCh37] Chr9:116048977..116439182 [NCBI36] Chr9:9q32 |
uncertain significance |
GRCh38/hg38 9q32(chr9:114270395-114677524)x3 | copy number gain | See cases [RCV000052237] | Chr9:114270395..114677524 [GRCh38] Chr9:117032675..117439804 [GRCh37] Chr9:116072496..116479625 [NCBI36] Chr9:9q32 |
uncertain significance |
GRCh38/hg38 9q22.33-33.1(chr9:99349916-115767475)x1 | copy number loss | See cases [RCV000052921] | Chr9:99349916..115767475 [GRCh38] Chr9:102112198..118529754 [GRCh37] Chr9:101152019..117569575 [NCBI36] Chr9:9q22.33-33.1 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3 | copy number gain | See cases [RCV000053746] | Chr9:193412..138114463 [GRCh38] Chr9:214367..141008915 [GRCh37] Chr9:204367..140128736 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|See cases [RCV000053748] | Chr9:193412..138179445 [GRCh38] Chr9:266045..141073897 [GRCh37] Chr9:256045..140193718 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3 | copy number gain | See cases [RCV000053745] | Chr9:193412..138124532 [GRCh38] Chr9:204193..141018984 [GRCh37] Chr9:194193..140138805 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
NM_032888.3(COL27A1):c.1593T>C (p.Thr531=) | single nucleotide variant | Malignant melanoma [RCV000068502] | Chr9:114169148 [GRCh38] Chr9:116931428 [GRCh37] Chr9:115971249 [NCBI36] Chr9:9q32 |
not provided |
NM_032888.3(COL27A1):c.3382C>T (p.Pro1128Ser) | single nucleotide variant | Malignant melanoma [RCV000061865] | Chr9:114265464 [GRCh38] Chr9:117027744 [GRCh37] Chr9:116067565 [NCBI36] Chr9:9q32 |
not provided |
GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445) | copy number gain | See cases [RCV000133791] | Chr9:204193..138179445 [GRCh38] Chr9:204193..141073897 [GRCh37] Chr9:194193..140193718 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9q32(chr9:114246889-114637174)x3 | copy number gain | See cases [RCV000138841] | Chr9:114246889..114637174 [GRCh38] Chr9:117009169..117399454 [GRCh37] Chr9:116048990..116439275 [NCBI36] Chr9:9q32 |
likely benign |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3 | copy number gain | See cases [RCV000138783] | Chr9:193412..138124524 [GRCh38] Chr9:204090..141018976 [GRCh37] Chr9:194090..140138797 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3 | copy number gain | See cases [RCV000138962] | Chr9:193412..138159073 [GRCh38] Chr9:204104..141053525 [GRCh37] Chr9:194104..140173346 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic|conflicting data from submitters |
GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3 | copy number gain | See cases [RCV000139207] | Chr9:193412..138159073 [GRCh38] Chr9:68420641..141053525 [GRCh37] Chr9:67910461..140173346 [NCBI36] Chr9:9p11.2-q34.3 |
pathogenic |
GRCh38/hg38 9q31.2-33.1(chr9:107530314-117965944)x1 | copy number loss | See cases [RCV000140794] | Chr9:107530314..117965944 [GRCh38] Chr9:110292595..120728222 [GRCh37] Chr9:109332416..119768043 [NCBI36] Chr9:9q31.2-33.1 |
pathogenic |
GRCh38/hg38 9q32(chr9:114193726-114677465)x3 | copy number gain | See cases [RCV000140795] | Chr9:114193726..114677465 [GRCh38] Chr9:116956006..117439745 [GRCh37] Chr9:115995827..116479566 [NCBI36] Chr9:9q32 |
benign |
GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 | copy number gain | See cases [RCV000141876] | Chr9:203861..138125937 [GRCh38] Chr9:203861..141020389 [GRCh37] Chr9:193861..140140210 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3 | copy number gain | See cases [RCV000143476] | Chr9:203862..138125937 [GRCh38] Chr9:203862..141020389 [GRCh37] Chr9:193862..140140210 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1 | copy number loss | See cases [RCV000148264] | Chr9:99138048..115011033 [GRCh38] Chr9:101900330..117773312 [GRCh37] Chr9:100940151..116813133 [NCBI36] Chr9:9q22.33-33.1 |
pathogenic |
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 | copy number gain | See cases [RCV000148113] | Chr9:193412..138179445 [GRCh38] Chr9:204193..141073897 [GRCh37] Chr9:194193..140193718 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3 | copy number gain | See cases [RCV000240081] | Chr9:163131..141122114 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9q32(chr9:116978042-117187294)x1 | copy number loss | See cases [RCV000240427] | Chr9:116978042..117187294 [GRCh37] Chr9:9q32 |
uncertain significance |
GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311) | copy number loss | Distal tetrasomy 15q [RCV002280776] | Chr9:19356861..119513311 [GRCh37] Chr9:9p22.1-q33.1 |
uncertain significance |
NM_032888.4(COL27A1):c.364C>T (p.Arg122Cys) | single nucleotide variant | not provided [RCV000593048] | Chr9:114167919 [GRCh38] Chr9:116930199 [GRCh37] Chr9:9q32 |
conflicting interpretations of pathogenicity|uncertain significance |
GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407) | copy number gain | See cases [RCV000449375] | Chr9:62525..141006407 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9q31.3-33.1(chr9:111348809-118687200)x1 | copy number loss | See cases [RCV000449308] | Chr9:111348809..118687200 [GRCh37] Chr9:9q31.3-33.1 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 | copy number gain | not specified [RCV003986800] | Chr9:203861..141020389 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9q31.1-33.3(chr9:104604851-126253089)x1 | copy number loss | See cases [RCV000447763] | Chr9:104604851..126253089 [GRCh37] Chr9:9q31.1-33.3 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:203864-141020389)x3 | copy number gain | See cases [RCV000448978] | Chr9:203864..141020389 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9q31.3-33.2(chr9:114299780-123267736)x1 | copy number loss | See cases [RCV000511049] | Chr9:114299780..123267736 [GRCh37] Chr9:9q31.3-33.2 |
pathogenic |
NM_032888.4(COL27A1):c.3062G>A (p.Gly1021Asp) | single nucleotide variant | Inborn genetic diseases [RCV000624416] | Chr9:114252621 [GRCh38] Chr9:117014901 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.1259G>A (p.Arg420His) | single nucleotide variant | Inborn genetic diseases [RCV003255107] | Chr9:114168814 [GRCh38] Chr9:116931094 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1907C>T (p.Pro636Leu) | single nucleotide variant | Inborn genetic diseases [RCV003255134] | Chr9:114169462 [GRCh38] Chr9:116931742 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3008G>C (p.Gly1003Ala) | single nucleotide variant | Inborn genetic diseases [RCV003249821] | Chr9:114250643 [GRCh38] Chr9:117012923 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1952G>A (p.Arg651His) | single nucleotide variant | not provided [RCV000595671] | Chr9:114178334 [GRCh38] Chr9:116940614 [GRCh37] Chr9:9q32 |
uncertain significance |
GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928) | copy number gain | Global developmental delay [RCV000626548] | Chr9:71069743..140999928 [GRCh37] Chr9:9q21.11-34.3 |
likely pathogenic |
NM_032888.4(COL27A1):c.5185C>T (p.Gln1729Ter) | single nucleotide variant | Inborn genetic diseases [RCV000624672] | Chr9:114307746 [GRCh38] Chr9:117070026 [GRCh37] Chr9:9q32 |
pathogenic|likely pathogenic |
NM_032888.4(COL27A1):c.371del (p.Leu124fs) | deletion | Inborn genetic diseases [RCV000622631] | Chr9:114167926 [GRCh38] Chr9:116930206 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3110G>A (p.Gly1037Asp) | single nucleotide variant | not provided [RCV000597786] | Chr9:114252901 [GRCh38] Chr9:117015181 [GRCh37] Chr9:9q32 |
uncertain significance |
GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389) | copy number gain | See cases [RCV000512392] | Chr9:203862..141020389 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
NM_032888.4(COL27A1):c.241C>T (p.Arg81Trp) | single nucleotide variant | Steel syndrome [RCV000660583]|not provided [RCV001855390] | Chr9:114167796 [GRCh38] Chr9:116930076 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.521_528del (p.Cys174fs) | deletion | Steel syndrome [RCV000677093] | Chr9:114168076..114168083 [GRCh38] Chr9:116930356..116930363 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3556-2A>G | single nucleotide variant | Steel syndrome [RCV000677205] | Chr9:114270726 [GRCh38] Chr9:117033006 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2119C>T (p.Arg707Ter) | single nucleotide variant | Steel syndrome [RCV000677092]|not provided [RCV002531384] | Chr9:114196007 [GRCh38] Chr9:116958287 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2619+62T>C | single nucleotide variant | Steel syndrome [RCV001543783] | Chr9:114235714 [GRCh38] Chr9:116997994 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1883G>A (p.Gly628Glu) | single nucleotide variant | Steel syndrome [RCV001559267] | Chr9:114169438 [GRCh38] Chr9:116931718 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4206+39A>G | single nucleotide variant | Steel syndrome [RCV001543920] | Chr9:114289334 [GRCh38] Chr9:117051614 [GRCh37] Chr9:9q32 |
benign |
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141122247)x3 | copy number gain | not provided [RCV000748055] | Chr9:10590..141122247 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9q31.3-33.3(chr9:113083182-126779494)x1 | copy number loss | not provided [RCV000748606] | Chr9:113083182..126779494 [GRCh37] Chr9:9q31.3-33.3 |
pathogenic |
GRCh37/hg19 9q32(chr9:117054195-117502242)x3 | copy number gain | not provided [RCV000748633] | Chr9:117054195..117502242 [GRCh37] Chr9:9q32 |
benign |
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3 | copy number gain | not provided [RCV000748053] | Chr9:10590..141107672 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:46587-141066491)x3 | copy number gain | not provided [RCV000748063] | Chr9:46587..141066491 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141114095)x2 | copy number gain | not provided [RCV000748054] | Chr9:10590..141114095 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
NM_032888.4(COL27A1):c.4074G>A (p.Gly1358=) | single nucleotide variant | not provided [RCV000976906] | Chr9:114288731 [GRCh38] Chr9:117051011 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2724C>T (p.Pro908=) | single nucleotide variant | COL27A1-related condition [RCV003902978]|not provided [RCV000918286] | Chr9:114237712 [GRCh38] Chr9:116999992 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.739G>A (p.Gly247Arg) | single nucleotide variant | COL27A1-related condition [RCV003950857]|Inborn genetic diseases [RCV003169307]|not provided [RCV000918489] | Chr9:114168294 [GRCh38] Chr9:116930574 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.3747C>T (p.Gly1249=) | single nucleotide variant | COL27A1-related condition [RCV003923229]|not provided [RCV000916238] | Chr9:114282306 [GRCh38] Chr9:117044586 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3758G>A (p.Arg1253His) | single nucleotide variant | Steel syndrome [RCV002495521]|not provided [RCV000916239] | Chr9:114282317 [GRCh38] Chr9:117044597 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2916C>T (p.Pro972=) | single nucleotide variant | not provided [RCV000940999] | Chr9:114243542 [GRCh38] Chr9:117005822 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3063C>A (p.Gly1021=) | single nucleotide variant | not provided [RCV000896923] | Chr9:114252622 [GRCh38] Chr9:117014902 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2071-95C>T | single nucleotide variant | Steel syndrome [RCV001543778] | Chr9:114195864 [GRCh38] Chr9:116958144 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2071-25C>T | single nucleotide variant | Steel syndrome [RCV001543779] | Chr9:114195934 [GRCh38] Chr9:116958214 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1160del (p.Pro387fs) | deletion | not provided [RCV001546153] | Chr9:114168714 [GRCh38] Chr9:116930994 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3933+128G>A | single nucleotide variant | Steel syndrome [RCV001543915] | Chr9:114283890 [GRCh38] Chr9:117046170 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4476+18A>G | single nucleotide variant | Steel syndrome [RCV001543921]|not provided [RCV002071968] | Chr9:114290935 [GRCh38] Chr9:117053215 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2566-10G>A | single nucleotide variant | not provided [RCV000978418] | Chr9:114235589 [GRCh38] Chr9:116997869 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5197A>G (p.Lys1733Glu) | single nucleotide variant | COL27A1-related condition [RCV003923237]|not provided [RCV000916525] | Chr9:114307758 [GRCh38] Chr9:117070038 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4519C>T (p.Arg1507Ter) | single nucleotide variant | Steel syndrome [RCV001644994]|not provided [RCV003770808] | Chr9:114292145 [GRCh38] Chr9:117054425 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4152+24C>A | single nucleotide variant | Steel syndrome [RCV001543918] | Chr9:114288991 [GRCh38] Chr9:117051271 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4846-17G>A | single nucleotide variant | Steel syndrome [RCV001543924]|not provided [RCV002071969] | Chr9:114302065 [GRCh38] Chr9:117064345 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.*31C>T | single nucleotide variant | Steel syndrome [RCV001543997] | Chr9:114310726 [GRCh38] Chr9:117073006 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.370C>G (p.Leu124Val) | single nucleotide variant | COL27A1-related condition [RCV003943141]|not provided [RCV000965115] | Chr9:114167925 [GRCh38] Chr9:116930205 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.1045C>T (p.Arg349Cys) | single nucleotide variant | not provided [RCV000973437] | Chr9:114168600 [GRCh38] Chr9:116930880 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.672C>T (p.Val224=) | single nucleotide variant | not provided [RCV000943330] | Chr9:114168227 [GRCh38] Chr9:116930507 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.915C>A (p.Pro305=) | single nucleotide variant | not provided [RCV000982477] | Chr9:114168470 [GRCh38] Chr9:116930750 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3715C>T (p.Arg1239Trp) | single nucleotide variant | not provided [RCV000905541] | Chr9:114275766 [GRCh38] Chr9:117038046 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2766C>T (p.Gly922=) | single nucleotide variant | not provided [RCV000947196] | Chr9:114240258 [GRCh38] Chr9:117002538 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4836C>T (p.Pro1612=) | single nucleotide variant | not provided [RCV000927452] | Chr9:114301708 [GRCh38] Chr9:117063988 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3702C>T (p.Gly1234=) | single nucleotide variant | not provided [RCV000971772] | Chr9:114275753 [GRCh38] Chr9:117038033 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.938C>T (p.Ala313Val) | single nucleotide variant | Inborn genetic diseases [RCV002537536]|not provided [RCV000900366] | Chr9:114168493 [GRCh38] Chr9:116930773 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.3276G>A (p.Pro1092=) | single nucleotide variant | not provided [RCV000943914] | Chr9:114264950 [GRCh38] Chr9:117027230 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.815T>C (p.Leu272Ser) | single nucleotide variant | not provided [RCV000971003] | Chr9:114168370 [GRCh38] Chr9:116930650 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2856G>A (p.Gly952=) | single nucleotide variant | not provided [RCV000943031] | Chr9:114242207 [GRCh38] Chr9:117004487 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5058C>T (p.Pro1686=) | single nucleotide variant | not provided [RCV000966211] | Chr9:114306639 [GRCh38] Chr9:117068919 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.3772-8T>C | single nucleotide variant | not provided [RCV000945132] | Chr9:114282449 [GRCh38] Chr9:117044729 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1041G>C (p.Thr347=) | single nucleotide variant | COL27A1-related condition [RCV003923208]|not provided [RCV000914635] | Chr9:114168596 [GRCh38] Chr9:116930876 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.2709C>T (p.Pro903=) | single nucleotide variant | not provided [RCV000943244] | Chr9:114237697 [GRCh38] Chr9:116999977 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2115G>A (p.Pro705=) | single nucleotide variant | not provided [RCV000880879] | Chr9:114196003 [GRCh38] Chr9:116958283 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3535C>G (p.Gln1179Glu) | single nucleotide variant | COL27A1-related condition [RCV003958368]|Inborn genetic diseases [RCV002540874]|not provided [RCV000914549] | Chr9:114269274 [GRCh38] Chr9:117031554 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.3716G>A (p.Arg1239Gln) | single nucleotide variant | not provided [RCV000914609] | Chr9:114275767 [GRCh38] Chr9:117038047 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3988-8G>A | single nucleotide variant | not provided [RCV000975536] | Chr9:114288447 [GRCh38] Chr9:117050727 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2858C>T (p.Pro953Leu) | single nucleotide variant | COL27A1-related condition [RCV003920501]|not provided [RCV000880111] | Chr9:114242209 [GRCh38] Chr9:117004489 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2295C>T (p.Phe765=) | single nucleotide variant | not provided [RCV000901046] | Chr9:114209701 [GRCh38] Chr9:116971981 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3198C>A (p.Gly1066=) | single nucleotide variant | not provided [RCV000942192] | Chr9:114264357 [GRCh38] Chr9:117026637 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.258G>A (p.Thr86=) | single nucleotide variant | not provided [RCV000965793] | Chr9:114167813 [GRCh38] Chr9:116930093 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1310C>T (p.Pro437Leu) | single nucleotide variant | COL27A1-related condition [RCV003960796]|not provided [RCV000968159] | Chr9:114168865 [GRCh38] Chr9:116931145 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4455A>C (p.Ala1485=) | single nucleotide variant | not provided [RCV000983226] | Chr9:114290896 [GRCh38] Chr9:117053176 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3556-9C>A | single nucleotide variant | not provided [RCV000943594] | Chr9:114270719 [GRCh38] Chr9:117032999 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.117C>A (p.Thr39=) | single nucleotide variant | not provided [RCV000923403] | Chr9:114162769 [GRCh38] Chr9:116925049 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2121A>G (p.Arg707=) | single nucleotide variant | not provided [RCV000928816] | Chr9:114196009 [GRCh38] Chr9:116958289 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1030T>A (p.Ser344Thr) | single nucleotide variant | not provided [RCV000943572] | Chr9:114168585 [GRCh38] Chr9:116930865 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2170-9C>G | single nucleotide variant | not provided [RCV000982810] | Chr9:114205750 [GRCh38] Chr9:116968030 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1668C>T (p.Pro556=) | single nucleotide variant | not provided [RCV000937287] | Chr9:114169223 [GRCh38] Chr9:116931503 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3281G>A (p.Arg1094Gln) | single nucleotide variant | COL27A1-related condition [RCV003936109]|not provided [RCV000971004] | Chr9:114264955 [GRCh38] Chr9:117027235 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.4255G>A (p.Val1419Ile) | single nucleotide variant | not provided [RCV000899853] | Chr9:114290106 [GRCh38] Chr9:117052386 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.216G>A (p.Ser72=) | single nucleotide variant | not provided [RCV000944272] | Chr9:114167771 [GRCh38] Chr9:116930051 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1963-7C>G | single nucleotide variant | not provided [RCV000884548] | Chr9:114183015 [GRCh38] Chr9:116945295 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.612G>A (p.Pro204=) | single nucleotide variant | COL27A1-related condition [RCV003960410]|not provided [RCV000922282] | Chr9:114168167 [GRCh38] Chr9:116930447 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.4831C>A (p.Arg1611=) | single nucleotide variant | not provided [RCV000879425] | Chr9:114301703 [GRCh38] Chr9:117063983 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1727G>C (p.Ser576Thr) | single nucleotide variant | Inborn genetic diseases [RCV003169219]|not provided [RCV000882011] | Chr9:114169282 [GRCh38] Chr9:116931562 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.1620A>G (p.Glu540=) | single nucleotide variant | COL27A1-related condition [RCV003942961]|not provided [RCV000941846] | Chr9:114169175 [GRCh38] Chr9:116931455 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2301G>A (p.Leu767=) | single nucleotide variant | not provided [RCV000927763] | Chr9:114209707 [GRCh38] Chr9:116971987 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2323-8C>T | single nucleotide variant | COL27A1-related condition [RCV003960463]|not provided [RCV000927764] | Chr9:114210974 [GRCh38] Chr9:116973254 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4350C>T (p.Asp1450=) | single nucleotide variant | not provided [RCV000920882] | Chr9:114290313 [GRCh38] Chr9:117052593 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5253C>T (p.Phe1751=) | single nucleotide variant | not provided [RCV000983197] | Chr9:114309295 [GRCh38] Chr9:117071575 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4066G>C (p.Asp1356His) | single nucleotide variant | Steel syndrome [RCV002505300]|not provided [RCV000899864] | Chr9:114288723 [GRCh38] Chr9:117051003 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4795T>C (p.Leu1599=) | single nucleotide variant | not provided [RCV000944314] | Chr9:114301448 [GRCh38] Chr9:117063728 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5034G>A (p.Thr1678=) | single nucleotide variant | not provided [RCV000882172] | Chr9:114306615 [GRCh38] Chr9:117068895 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2835+6A>G | single nucleotide variant | COL27A1-related condition [RCV003968027]|not provided [RCV000884730] | Chr9:114240493 [GRCh38] Chr9:117002773 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3690C>T (p.Pro1230=) | single nucleotide variant | not provided [RCV000922325] | Chr9:114275741 [GRCh38] Chr9:117038021 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2988G>A (p.Met996Ile) | single nucleotide variant | COL27A1-related condition [RCV003913249]|not provided [RCV000948357] | Chr9:114250623 [GRCh38] Chr9:117012903 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1116T>A (p.Pro372=) | single nucleotide variant | not provided [RCV000981412] | Chr9:114168671 [GRCh38] Chr9:116930951 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.93del (p.Phe32fs) | deletion | Steel syndrome [RCV000995715] | Chr9:114162745 [GRCh38] Chr9:116925025 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2409G>A (p.Leu803=) | single nucleotide variant | Steel syndrome [RCV001072106] | Chr9:114219832 [GRCh38] Chr9:116982112 [GRCh37] Chr9:9q32 |
likely pathogenic |
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3 | copy number gain | not provided [RCV000845900] | Chr9:203861..141020388 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
NM_032888.4(COL27A1):c.2181A>G (p.Gly727=) | single nucleotide variant | not provided [RCV000942704] | Chr9:114205770 [GRCh38] Chr9:116968050 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5190G>A (p.Thr1730=) | single nucleotide variant | not provided [RCV000978256] | Chr9:114307751 [GRCh38] Chr9:117070031 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3880-10C>T | single nucleotide variant | not provided [RCV000917319] | Chr9:114283699 [GRCh38] Chr9:117045979 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2682C>T (p.Val894=) | single nucleotide variant | not provided [RCV000979066] | Chr9:114237670 [GRCh38] Chr9:116999950 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1135A>T (p.Ile379Phe) | single nucleotide variant | COL27A1-related condition [RCV003903135]|Steel syndrome [RCV002479084]|not provided [RCV000941416] | Chr9:114168690 [GRCh38] Chr9:116930970 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5571G>A (p.Ala1857=) | single nucleotide variant | not provided [RCV000944780] | Chr9:114310683 [GRCh38] Chr9:117072963 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4194G>T (p.Ser1398=) | single nucleotide variant | not provided [RCV000977158] | Chr9:114289283 [GRCh38] Chr9:117051563 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1413G>A (p.Pro471=) | single nucleotide variant | not provided [RCV000941547] | Chr9:114168968 [GRCh38] Chr9:116931248 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5217+6C>T | single nucleotide variant | COL27A1-related condition [RCV003933215]|not provided [RCV000941553] | Chr9:114307784 [GRCh38] Chr9:117070064 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.178G>A (p.Gly60Arg) | single nucleotide variant | not provided [RCV000963928] | Chr9:114167733 [GRCh38] Chr9:116930013 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3972A>T (p.Gly1324=) | single nucleotide variant | not provided [RCV000897144] | Chr9:114284762 [GRCh38] Chr9:117047042 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.483C>T (p.Leu161=) | single nucleotide variant | not provided [RCV000941880] | Chr9:114168038 [GRCh38] Chr9:116930318 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2859G>T (p.Pro953=) | single nucleotide variant | not provided [RCV000977379] | Chr9:114242210 [GRCh38] Chr9:117004490 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4761G>A (p.Pro1587=) | single nucleotide variant | not provided [RCV000918547] | Chr9:114301289 [GRCh38] Chr9:117063569 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1194G>A (p.Lys398=) | single nucleotide variant | not provided [RCV000980727] | Chr9:114168749 [GRCh38] Chr9:116931029 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1530A>G (p.Pro510=) | single nucleotide variant | not provided [RCV000980746] | Chr9:114169085 [GRCh38] Chr9:116931365 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.840G>T (p.Gly280=) | single nucleotide variant | not provided [RCV000967137] | Chr9:114168395 [GRCh38] Chr9:116930675 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4326A>G (p.Gly1442=) | single nucleotide variant | not provided [RCV000944835] | Chr9:114290289 [GRCh38] Chr9:117052569 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.893C>T (p.Thr298Ile) | single nucleotide variant | Inborn genetic diseases [RCV002542174]|not provided [RCV000922827] | Chr9:114168448 [GRCh38] Chr9:116930728 [GRCh37] Chr9:9q32 |
benign|uncertain significance |
NM_032888.4(COL27A1):c.5218-5T>C | single nucleotide variant | not provided [RCV000897713] | Chr9:114309255 [GRCh38] Chr9:117071535 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.141C>T (p.Asp47=) | single nucleotide variant | not provided [RCV000942274] | Chr9:114167696 [GRCh38] Chr9:116929976 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.231G>A (p.Thr77=) | single nucleotide variant | not provided [RCV000943614] | Chr9:114167786 [GRCh38] Chr9:116930066 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2865G>C (p.Gly955=) | single nucleotide variant | not provided [RCV000982784] | Chr9:114242216 [GRCh38] Chr9:117004496 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5355C>T (p.Ala1785=) | single nucleotide variant | not provided [RCV000982797] | Chr9:114309397 [GRCh38] Chr9:117071677 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2199G>C (p.Gly733=) | single nucleotide variant | not provided [RCV000903291] | Chr9:114205788 [GRCh38] Chr9:116968068 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1653C>T (p.Pro551=) | single nucleotide variant | not provided [RCV000942353] | Chr9:114169208 [GRCh38] Chr9:116931488 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.133+9C>G | single nucleotide variant | not provided [RCV000943187] | Chr9:114162794 [GRCh38] Chr9:116925074 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.66G>T (p.Gly22=) | single nucleotide variant | not provided [RCV000931730] | Chr9:114162718 [GRCh38] Chr9:116924998 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4818C>T (p.Pro1606=) | single nucleotide variant | not provided [RCV000918764] | Chr9:114301690 [GRCh38] Chr9:117063970 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4206+7G>A | single nucleotide variant | not provided [RCV000977217] | Chr9:114289302 [GRCh38] Chr9:117051582 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1163C>T (p.Thr388Ile) | single nucleotide variant | COL27A1-related condition [RCV003930697]|not provided [RCV000887424] | Chr9:114168718 [GRCh38] Chr9:116930998 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.5063G>A (p.Arg1688Gln) | single nucleotide variant | COL27A1-related condition [RCV003958108]|Steel syndrome [RCV001559266]|not provided [RCV000899078] | Chr9:114306644 [GRCh38] Chr9:117068924 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.2859G>A (p.Pro953=) | single nucleotide variant | not provided [RCV000982115] | Chr9:114242210 [GRCh38] Chr9:117004490 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3393+8C>A | single nucleotide variant | not provided [RCV000977611] | Chr9:114265483 [GRCh38] Chr9:117027763 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2058C>T (p.His686=) | single nucleotide variant | not provided [RCV000980059] | Chr9:114194445 [GRCh38] Chr9:116956725 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.843A>T (p.Ser281=) | single nucleotide variant | not provided [RCV000978715] | Chr9:114168398 [GRCh38] Chr9:116930678 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1782G>A (p.Pro594=) | single nucleotide variant | not provided [RCV000941032] | Chr9:114169337 [GRCh38] Chr9:116931617 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2815C>T (p.Arg939Cys) | single nucleotide variant | Inborn genetic diseases [RCV003169431]|not provided [RCV000942140] | Chr9:114240467 [GRCh38] Chr9:117002747 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.3195+7C>T | single nucleotide variant | not provided [RCV000943788] | Chr9:114258601 [GRCh38] Chr9:117020881 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1890G>A (p.Lys630=) | single nucleotide variant | not provided [RCV000922369] | Chr9:114169445 [GRCh38] Chr9:116931725 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.456C>T (p.His152=) | single nucleotide variant | not provided [RCV000900522] | Chr9:114168011 [GRCh38] Chr9:116930291 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3777C>G (p.Ala1259=) | single nucleotide variant | not provided [RCV000949328] | Chr9:114282462 [GRCh38] Chr9:117044742 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1052C>T (p.Ala351Val) | single nucleotide variant | Inborn genetic diseases [RCV003169333]|not provided [RCV000928644] | Chr9:114168607 [GRCh38] Chr9:116930887 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.2958G>T (p.Arg986=) | single nucleotide variant | not provided [RCV000977338] | Chr9:114245889 [GRCh38] Chr9:117008169 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4735C>T (p.Leu1579=) | single nucleotide variant | not provided [RCV000941107] | Chr9:114301105 [GRCh38] Chr9:117063385 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4131G>A (p.Lys1377=) | single nucleotide variant | not provided [RCV000980349] | Chr9:114288946 [GRCh38] Chr9:117051226 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2622G>T (p.Gly874=) | single nucleotide variant | COL27A1-related condition [RCV003903057]|not provided [RCV000925758] | Chr9:114236983 [GRCh38] Chr9:116999263 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1101C>T (p.Ser367=) | single nucleotide variant | not provided [RCV000978856] | Chr9:114168656 [GRCh38] Chr9:116930936 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1289C>T (p.Pro430Leu) | single nucleotide variant | not provided [RCV000939963] | Chr9:114168844 [GRCh38] Chr9:116931124 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.543C>T (p.Val181=) | single nucleotide variant | not provided [RCV000980139] | Chr9:114168098 [GRCh38] Chr9:116930378 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3717+8T>C | single nucleotide variant | not provided [RCV000939219] | Chr9:114275776 [GRCh38] Chr9:117038056 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4872+8G>A | single nucleotide variant | not provided [RCV000977615] | Chr9:114302116 [GRCh38] Chr9:117064396 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.573C>T (p.Leu191=) | single nucleotide variant | not provided [RCV000885914] | Chr9:114168128 [GRCh38] Chr9:116930408 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1617G>A (p.Ser539=) | single nucleotide variant | not provided [RCV000885915] | Chr9:114169172 [GRCh38] Chr9:116931452 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1455T>C (p.Thr485=) | single nucleotide variant | not provided [RCV000886006] | Chr9:114169010 [GRCh38] Chr9:116931290 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.939G>A (p.Ala313=) | single nucleotide variant | not provided [RCV000963657] | Chr9:114168494 [GRCh38] Chr9:116930774 [GRCh37] Chr9:9q32 |
benign |
GRCh37/hg19 9q32(chr9:116642144-117613527)x1 | copy number loss | not provided [RCV001006255] | Chr9:116642144..117613527 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2040C>G (p.Leu680=) | single nucleotide variant | not provided [RCV000977007] | Chr9:114194427 [GRCh38] Chr9:116956707 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4530G>A (p.Glu1510=) | single nucleotide variant | not provided [RCV000977008] | Chr9:114292156 [GRCh38] Chr9:117054436 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4045-7C>T | single nucleotide variant | not provided [RCV000976711] | Chr9:114288695 [GRCh38] Chr9:117050975 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.393C>T (p.Leu131=) | single nucleotide variant | not provided [RCV000976714] | Chr9:114167948 [GRCh38] Chr9:116930228 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4809+1G>C | single nucleotide variant | not provided [RCV000793298] | Chr9:114301463 [GRCh38] Chr9:117063743 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4029G>A (p.Gly1343=) | single nucleotide variant | not provided [RCV000892943] | Chr9:114288496 [GRCh38] Chr9:117050776 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3196-1G>A | single nucleotide variant | not provided [RCV000801442] | Chr9:114264354 [GRCh38] Chr9:117026634 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2661G>A (p.Lys887=) | single nucleotide variant | not provided [RCV000976458] | Chr9:114237022 [GRCh38] Chr9:116999302 [GRCh37] Chr9:9q32 |
likely benign |
GRCh37/hg19 9q32(chr9:116936770-117450535)x3 | copy number gain | not provided [RCV000848120] | Chr9:116936770..117450535 [GRCh37] Chr9:9q32 |
uncertain significance |
GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3 | copy number gain | not provided [RCV000847808] | Chr9:71416475..141020389 [GRCh37] Chr9:9q21.11-34.3 |
pathogenic |
NM_032888.4(COL27A1):c.2877G>A (p.Leu959=) | single nucleotide variant | not provided [RCV000977891] | Chr9:114242228 [GRCh38] Chr9:117004508 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4045-6A>G | single nucleotide variant | not provided [RCV000978809] | Chr9:114288696 [GRCh38] Chr9:117050976 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.36A>G (p.Thr12=) | single nucleotide variant | not provided [RCV000942441] | Chr9:114155986 [GRCh38] Chr9:116918266 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.786C>T (p.Ser262=) | single nucleotide variant | not provided [RCV000941558] | Chr9:114168341 [GRCh38] Chr9:116930621 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2268+7G>A | single nucleotide variant | not provided [RCV000898305] | Chr9:114206303 [GRCh38] Chr9:116968583 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4059T>G (p.Asp1353Glu) | single nucleotide variant | not provided [RCV000891713] | Chr9:114288716 [GRCh38] Chr9:117050996 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4965G>A (p.Val1655=) | single nucleotide variant | not provided [RCV000959011] | Chr9:114306546 [GRCh38] Chr9:117068826 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3684G>A (p.Gly1228=) | single nucleotide variant | not provided [RCV000975879] | Chr9:114275735 [GRCh38] Chr9:117038015 [GRCh37] Chr9:9q32 |
likely benign |
GRCh37/hg19 9q31.3-32(chr9:113982711-117443628)x1 | copy number loss | not provided [RCV000847543] | Chr9:113982711..117443628 [GRCh37] Chr9:9q31.3-32 |
uncertain significance |
NM_032888.4(COL27A1):c.4938+2T>C | single nucleotide variant | not provided [RCV001221989] | Chr9:114304675 [GRCh38] Chr9:117066955 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.62+1del | deletion | Steel syndrome [RCV001780181]|not provided [RCV001242955] | Chr9:114156008 [GRCh38] Chr9:116918288 [GRCh37] Chr9:9q32 |
pathogenic|likely pathogenic |
NM_032888.4(COL27A1):c.1060C>T (p.Gln354Ter) | single nucleotide variant | not provided [RCV001222255] | Chr9:114168615 [GRCh38] Chr9:116930895 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2466+1G>T | single nucleotide variant | not provided [RCV001232694] | Chr9:114222268 [GRCh38] Chr9:116984548 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4012G>T (p.Ala1338Ser) | single nucleotide variant | Inborn genetic diseases [RCV003271796] | Chr9:114288479 [GRCh38] Chr9:117050759 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3075del (p.Lys1026fs) | deletion | Steel syndrome [RCV000995716] | Chr9:114252632 [GRCh38] Chr9:117014912 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2728-16C>G | single nucleotide variant | not provided [RCV003104796] | Chr9:114240204 [GRCh38] Chr9:117002484 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1840C>A (p.Leu614Met) | single nucleotide variant | not provided [RCV003105065] | Chr9:114169395 [GRCh38] Chr9:116931675 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1650C>T (p.Ser550=) | single nucleotide variant | not provided [RCV003106333] | Chr9:114169205 [GRCh38] Chr9:116931485 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.134-148G>A | single nucleotide variant | Steel syndrome [RCV001543745] | Chr9:114167541 [GRCh38] Chr9:116929821 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2016+26A>G | single nucleotide variant | Steel syndrome [RCV001543775] | Chr9:114183101 [GRCh38] Chr9:116945381 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3609+35C>T | single nucleotide variant | Steel syndrome [RCV001543788] | Chr9:114270816 [GRCh38] Chr9:117033096 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3610-121A>G | single nucleotide variant | Steel syndrome [RCV001543910] | Chr9:114275540 [GRCh38] Chr9:117037820 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3610-26T>C | single nucleotide variant | Steel syndrome [RCV001543911] | Chr9:114275635 [GRCh38] Chr9:117037915 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3718-99A>G | single nucleotide variant | Steel syndrome [RCV001543912] | Chr9:114282178 [GRCh38] Chr9:117044458 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4846-56T>C | single nucleotide variant | Steel syndrome [RCV001543923] | Chr9:114302026 [GRCh38] Chr9:117064306 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4285C>T (p.Arg1429Trp) | single nucleotide variant | not provided [RCV001561821] | Chr9:114290248 [GRCh38] Chr9:117052528 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2016+99A>C | single nucleotide variant | Steel syndrome [RCV001543776] | Chr9:114183174 [GRCh38] Chr9:116945454 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2016+192T>C | single nucleotide variant | Steel syndrome [RCV001543777] | Chr9:114183267 [GRCh38] Chr9:116945547 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2071-23C>T | single nucleotide variant | Steel syndrome [RCV001543780] | Chr9:114195936 [GRCh38] Chr9:116958216 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3250-136C>T | single nucleotide variant | Steel syndrome [RCV001543785] | Chr9:114264788 [GRCh38] Chr9:117027068 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4873-65C>T | single nucleotide variant | Steel syndrome [RCV001543996] | Chr9:114304543 [GRCh38] Chr9:117066823 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2524C>T (p.Leu842=) | single nucleotide variant | not provided [RCV000943601] | Chr9:114231825 [GRCh38] Chr9:116994105 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2159C>G (p.Pro720Arg) | single nucleotide variant | not provided [RCV000880982] | Chr9:114205136 [GRCh38] Chr9:116967416 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2715C>T (p.Pro905=) | single nucleotide variant | not provided [RCV000930213] | Chr9:114237703 [GRCh38] Chr9:116999983 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2892C>G (p.Gly964=) | single nucleotide variant | not provided [RCV000940957] | Chr9:114243518 [GRCh38] Chr9:117005798 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4728C>T (p.Leu1576=) | single nucleotide variant | COL27A1-related condition [RCV003903261]|not provided [RCV000954414] | Chr9:114301098 [GRCh38] Chr9:117063378 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3718-7T>C | single nucleotide variant | not provided [RCV000944672] | Chr9:114282270 [GRCh38] Chr9:117044550 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1815G>A (p.Thr605=) | single nucleotide variant | not provided [RCV000931667] | Chr9:114169370 [GRCh38] Chr9:116931650 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4071C>T (p.Arg1357=) | single nucleotide variant | COL27A1-related condition [RCV003978090]|not provided [RCV000932431] | Chr9:114288728 [GRCh38] Chr9:117051008 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.785C>A (p.Ser262Tyr) | single nucleotide variant | not provided [RCV000954412] | Chr9:114168340 [GRCh38] Chr9:116930620 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.793G>A (p.Ala265Thr) | single nucleotide variant | not provided [RCV000954413] | Chr9:114168348 [GRCh38] Chr9:116930628 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3453G>A (p.Pro1151=) | single nucleotide variant | not provided [RCV000931735] | Chr9:114267509 [GRCh38] Chr9:117029789 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5475C>T (p.Phe1825=) | single nucleotide variant | not provided [RCV000931744] | Chr9:114310587 [GRCh38] Chr9:117072867 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.62+9G>T | single nucleotide variant | not provided [RCV000977326] | Chr9:114156021 [GRCh38] Chr9:116918301 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.993C>T (p.Asn331=) | single nucleotide variant | not provided [RCV000931764] | Chr9:114168548 [GRCh38] Chr9:116930828 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4206+8G>A | single nucleotide variant | not provided [RCV000916559] | Chr9:114289303 [GRCh38] Chr9:117051583 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.681T>C (p.Asn227=) | single nucleotide variant | not provided [RCV000977513] | Chr9:114168236 [GRCh38] Chr9:116930516 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-3T>C | single nucleotide variant | COL27A1-related condition [RCV003930540]|not provided [RCV000881334] | Chr9:114250612 [GRCh38] Chr9:117012892 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.2535C>T (p.Ser845=) | single nucleotide variant | not provided [RCV000975564] | Chr9:114231836 [GRCh38] Chr9:116994116 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1854G>A (p.Thr618=) | single nucleotide variant | not provided [RCV000959096] | Chr9:114169409 [GRCh38] Chr9:116931689 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.276C>T (p.Ala92=) | single nucleotide variant | not provided [RCV000887423] | Chr9:114167831 [GRCh38] Chr9:116930111 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3524C>A (p.Thr1175Asn) | single nucleotide variant | Inborn genetic diseases [RCV003169278]|not provided [RCV000909271] | Chr9:114269263 [GRCh38] Chr9:117031543 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.3088-4G>A | single nucleotide variant | not provided [RCV000914781] | Chr9:114252875 [GRCh38] Chr9:117015155 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2748C>T (p.Gly916=) | single nucleotide variant | not provided [RCV000975851] | Chr9:114240240 [GRCh38] Chr9:117002520 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2958G>A (p.Arg986=) | single nucleotide variant | not provided [RCV000930593] | Chr9:114245889 [GRCh38] Chr9:117008169 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1902C>G (p.Gly634=) | single nucleotide variant | not provided [RCV000978022] | Chr9:114169457 [GRCh38] Chr9:116931737 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2970G>A (p.Val990=) | single nucleotide variant | not provided [RCV000941410] | Chr9:114245901 [GRCh38] Chr9:117008181 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.5218-4A>G | single nucleotide variant | not provided [RCV000929885] | Chr9:114309256 [GRCh38] Chr9:117071536 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.63-4C>A | single nucleotide variant | not provided [RCV000909377] | Chr9:114162711 [GRCh38] Chr9:116924991 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.399C>A (p.Gly133=) | single nucleotide variant | not provided [RCV000928775] | Chr9:114167954 [GRCh38] Chr9:116930234 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3934-6C>G | single nucleotide variant | not provided [RCV000910285] | Chr9:114284718 [GRCh38] Chr9:117046998 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1041G>A (p.Thr347=) | single nucleotide variant | not provided [RCV000976333] | Chr9:114168596 [GRCh38] Chr9:116930876 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5168A>G (p.Asn1723Ser) | single nucleotide variant | COL27A1-related condition [RCV003930649]|not provided [RCV000885623] | Chr9:114307729 [GRCh38] Chr9:117070009 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.303G>A (p.Val101=) | single nucleotide variant | COL27A1-related condition [RCV003933172]|not provided [RCV000932858] | Chr9:114167858 [GRCh38] Chr9:116930138 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.264C>T (p.Thr88=) | single nucleotide variant | not provided [RCV000937498] | Chr9:114167819 [GRCh38] Chr9:116930099 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1963-7C>T | single nucleotide variant | not provided [RCV000932126] | Chr9:114183015 [GRCh38] Chr9:116945295 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1655G>A (p.Arg552Gln) | single nucleotide variant | COL27A1-related condition [RCV003940822]|not provided [RCV000898878] | Chr9:114169210 [GRCh38] Chr9:116931490 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.408C>T (p.Val136=) | single nucleotide variant | not provided [RCV000951103] | Chr9:114167963 [GRCh38] Chr9:116930243 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.5517C>T (p.Asp1839=) | single nucleotide variant | not provided [RCV000930081] | Chr9:114310629 [GRCh38] Chr9:117072909 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1071G>A (p.Gln357=) | single nucleotide variant | not provided [RCV000982476] | Chr9:114168626 [GRCh38] Chr9:116930906 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.459C>T (p.Asp153=) | single nucleotide variant | not provided [RCV000921341] | Chr9:114168014 [GRCh38] Chr9:116930294 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4440C>T (p.Ala1480=) | single nucleotide variant | not provided [RCV000930113] | Chr9:114290881 [GRCh38] Chr9:117053161 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3555+10A>G | single nucleotide variant | not provided [RCV000983291] | Chr9:114269304 [GRCh38] Chr9:117031584 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1290G>A (p.Pro430=) | single nucleotide variant | not provided [RCV000920936] | Chr9:114168845 [GRCh38] Chr9:116931125 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1654C>A (p.Arg552=) | single nucleotide variant | not provided [RCV000910499] | Chr9:114169209 [GRCh38] Chr9:116931489 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2405G>A (p.Gly802Glu) | single nucleotide variant | Steel syndrome [RCV001090006] | Chr9:114219828 [GRCh38] Chr9:116982108 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2521G>A (p.Gly841Arg) | single nucleotide variant | Steel syndrome [RCV001007654] | Chr9:114231822 [GRCh38] Chr9:116994102 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.554dup (p.His186fs) | duplication | not provided [RCV001209714] | Chr9:114168106..114168107 [GRCh38] Chr9:116930386..116930387 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.619G>A (p.Val207Ile) | single nucleotide variant | COL27A1-related condition [RCV003968401]|not provided [RCV000911188] | Chr9:114168174 [GRCh38] Chr9:116930454 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2113C>T (p.Pro705Ser) | single nucleotide variant | COL27A1-related condition [RCV003975606]|Steel syndrome [RCV002495381]|not provided [RCV000889204] | Chr9:114196001 [GRCh38] Chr9:116958281 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.3772-9C>T | single nucleotide variant | not provided [RCV000935913] | Chr9:114282448 [GRCh38] Chr9:117044728 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.304C>T (p.Leu102=) | single nucleotide variant | not provided [RCV000890362] | Chr9:114167859 [GRCh38] Chr9:116930139 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4905G>A (p.Thr1635=) | single nucleotide variant | not provided [RCV000912289] | Chr9:114304640 [GRCh38] Chr9:117066920 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4320C>T (p.Ile1440=) | single nucleotide variant | not provided [RCV000890571] | Chr9:114290283 [GRCh38] Chr9:117052563 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3195+8G>A | single nucleotide variant | not provided [RCV000956740] | Chr9:114258602 [GRCh38] Chr9:117020882 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4539G>A (p.Thr1513=) | single nucleotide variant | not provided [RCV000934236] | Chr9:114292165 [GRCh38] Chr9:117054445 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.152G>A (p.Arg51Gln) | single nucleotide variant | not provided [RCV000890901] | Chr9:114167707 [GRCh38] Chr9:116929987 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.405G>A (p.Thr135=) | single nucleotide variant | not provided [RCV000890902] | Chr9:114167960 [GRCh38] Chr9:116930240 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1032T>C (p.Ser344=) | single nucleotide variant | not provided [RCV000890903] | Chr9:114168587 [GRCh38] Chr9:116930867 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.397G>A (p.Gly133Ser) | single nucleotide variant | not provided [RCV000911834] | Chr9:114167952 [GRCh38] Chr9:116930232 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2547C>T (p.Pro849=) | single nucleotide variant | not provided [RCV000912944] | Chr9:114231848 [GRCh38] Chr9:116994128 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2466+10T>C | single nucleotide variant | not provided [RCV000912792] | Chr9:114222277 [GRCh38] Chr9:116984557 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4806G>A (p.Pro1602=) | single nucleotide variant | not provided [RCV000912832] | Chr9:114301459 [GRCh38] Chr9:117063739 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.63-214A>G | single nucleotide variant | Steel syndrome [RCV001543744] | Chr9:114162501 [GRCh38] Chr9:116924781 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3250-39A>G | single nucleotide variant | Steel syndrome [RCV001543786] | Chr9:114264885 [GRCh38] Chr9:117027165 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4206+11C>G | single nucleotide variant | Steel syndrome [RCV001543919]|not provided [RCV002071967] | Chr9:114289306 [GRCh38] Chr9:117051586 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4584+52C>T | single nucleotide variant | Steel syndrome [RCV001543922] | Chr9:114292262 [GRCh38] Chr9:117054542 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4872+17C>G | single nucleotide variant | Steel syndrome [RCV001543925]|not provided [RCV002071970] | Chr9:114302125 [GRCh38] Chr9:117064405 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2980G>A (p.Gly994Arg) | single nucleotide variant | Inborn genetic diseases [RCV003253291] | Chr9:114250615 [GRCh38] Chr9:117012895 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2940A>G (p.Glu980=) | single nucleotide variant | not provided [RCV003106742] | Chr9:114245871 [GRCh38] Chr9:117008151 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3718-19G>T | single nucleotide variant | Steel syndrome [RCV001543913]|not provided [RCV002071966] | Chr9:114282258 [GRCh38] Chr9:117044538 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3628G>C (p.Gly1210Arg) | single nucleotide variant | not provided [RCV001539322] | Chr9:114275679 [GRCh38] Chr9:117037959 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2071-2A>G | single nucleotide variant | not provided [RCV001208366] | Chr9:114195957 [GRCh38] Chr9:116958237 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2809G>T (p.Gly937Ter) | single nucleotide variant | not provided [RCV001218148] | Chr9:114240461 [GRCh38] Chr9:117002741 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3917del (p.Gly1306fs) | deletion | not provided [RCV001046508] | Chr9:114283744 [GRCh38] Chr9:117046024 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4756-10T>A | single nucleotide variant | not provided [RCV003106770] | Chr9:114301274 [GRCh38] Chr9:117063554 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5189C>T (p.Thr1730Met) | single nucleotide variant | not provided [RCV002284854] | Chr9:114307750 [GRCh38] Chr9:117070030 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1963-277T>C | single nucleotide variant | Steel syndrome [RCV001543774] | Chr9:114182745 [GRCh38] Chr9:116945025 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2170-87T>C | single nucleotide variant | Steel syndrome [RCV001543782] | Chr9:114205672 [GRCh38] Chr9:116967952 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4967T>C (p.Leu1656Pro) | single nucleotide variant | Inborn genetic diseases [RCV002546632]|Steel syndrome [RCV001333376]|not provided [RCV002546631] | Chr9:114306548 [GRCh38] Chr9:117068828 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4979_4983del (p.Gly1660fs) | deletion | Steel syndrome [RCV001255864] | Chr9:114306557..114306561 [GRCh38] Chr9:117068837..117068841 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.5215A>G (p.Lys1739Glu) | single nucleotide variant | Steel syndrome [RCV001332721] | Chr9:114307776 [GRCh38] Chr9:117070056 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3439G>T (p.Gly1147Ter) | single nucleotide variant | Steel syndrome [RCV001332720]|not provided [RCV001865766] | Chr9:114266610 [GRCh38] Chr9:117028890 [GRCh37] Chr9:9q32 |
pathogenic|likely pathogenic |
NM_032888.4(COL27A1):c.1368A>G (p.Thr456=) | single nucleotide variant | not provided [RCV001415121] | Chr9:114168923 [GRCh38] Chr9:116931203 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4701+9C>T | single nucleotide variant | COL27A1-related condition [RCV003963270]|not provided [RCV001397197] | Chr9:114300696 [GRCh38] Chr9:117062976 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1572C>T (p.Pro524=) | single nucleotide variant | not provided [RCV001397369] | Chr9:114169127 [GRCh38] Chr9:116931407 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1656G>A (p.Arg552=) | single nucleotide variant | not provided [RCV001392527] | Chr9:114169211 [GRCh38] Chr9:116931491 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1495A>G (p.Arg499Gly) | single nucleotide variant | not provided [RCV001422983] | Chr9:114169050 [GRCh38] Chr9:116931330 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.543C>A (p.Val181=) | single nucleotide variant | not provided [RCV001394659] | Chr9:114168098 [GRCh38] Chr9:116930378 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.579T>C (p.Pro193=) | single nucleotide variant | not provided [RCV001392542] | Chr9:114168134 [GRCh38] Chr9:116930414 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2538G>C (p.Val846=) | single nucleotide variant | not provided [RCV001412716] | Chr9:114231839 [GRCh38] Chr9:116994119 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2319A>G (p.Glu773=) | single nucleotide variant | not provided [RCV001396952] | Chr9:114209725 [GRCh38] Chr9:116972005 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2467-6C>T | single nucleotide variant | not provided [RCV001414731] | Chr9:114231073 [GRCh38] Chr9:116993353 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1761C>T (p.Thr587=) | single nucleotide variant | not provided [RCV001414736] | Chr9:114169316 [GRCh38] Chr9:116931596 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1920G>A (p.Gly640=) | single nucleotide variant | not provided [RCV001391969] | Chr9:114178302 [GRCh38] Chr9:116940582 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3610-8C>T | single nucleotide variant | not provided [RCV001433090] | Chr9:114275653 [GRCh38] Chr9:117037933 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5265A>T (p.Leu1755=) | single nucleotide variant | not provided [RCV001395513] | Chr9:114309307 [GRCh38] Chr9:117071587 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1629G>A (p.Lys543=) | single nucleotide variant | not provided [RCV001395582] | Chr9:114169184 [GRCh38] Chr9:116931464 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4639-10C>T | single nucleotide variant | not provided [RCV001422237] | Chr9:114300615 [GRCh38] Chr9:117062895 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1401T>C (p.His467=) | single nucleotide variant | not provided [RCV001421263] | Chr9:114168956 [GRCh38] Chr9:116931236 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3738G>A (p.Gly1246=) | single nucleotide variant | not provided [RCV001433896] | Chr9:114282297 [GRCh38] Chr9:117044577 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3022G>A (p.Val1008Met) | single nucleotide variant | Inborn genetic diseases [RCV003298647]|not provided [RCV001395879] | Chr9:114250657 [GRCh38] Chr9:117012937 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1076T>C (p.Ile359Thr) | single nucleotide variant | not provided [RCV001421678] | Chr9:114168631 [GRCh38] Chr9:116930911 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1773A>C (p.Val591=) | single nucleotide variant | not provided [RCV001433308] | Chr9:114169328 [GRCh38] Chr9:116931608 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3406C>A (p.Pro1136Thr) | single nucleotide variant | Inborn genetic diseases [RCV002552693]|not provided [RCV001397533] | Chr9:114266577 [GRCh38] Chr9:117028857 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.3501+10G>A | single nucleotide variant | not provided [RCV001433311] | Chr9:114267567 [GRCh38] Chr9:117029847 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4059T>C (p.Asp1353=) | single nucleotide variant | not provided [RCV001433505] | Chr9:114288716 [GRCh38] Chr9:117050996 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4629C>T (p.Phe1543=) | single nucleotide variant | not provided [RCV001415075] | Chr9:114300114 [GRCh38] Chr9:117062394 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4179G>A (p.Pro1393=) | single nucleotide variant | not provided [RCV001397587] | Chr9:114289268 [GRCh38] Chr9:117051548 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3933+10T>A | single nucleotide variant | not provided [RCV001397634] | Chr9:114283772 [GRCh38] Chr9:117046052 [GRCh37] Chr9:9q32 |
likely benign |
NC_000009.11:g.(?_116956664)_(117267081_?)dup | duplication | not provided [RCV001339460] | Chr9:116956664..117267081 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3393+9C>G | single nucleotide variant | not provided [RCV001421304] | Chr9:114265484 [GRCh38] Chr9:117027764 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2442C>A (p.Gly814=) | single nucleotide variant | not provided [RCV001412374] | Chr9:114222243 [GRCh38] Chr9:116984523 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5130C>T (p.Asn1710=) | single nucleotide variant | not provided [RCV001421783] | Chr9:114307691 [GRCh38] Chr9:117069971 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5148C>T (p.Asp1716=) | single nucleotide variant | not provided [RCV001412348] | Chr9:114307709 [GRCh38] Chr9:117069989 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5220C>T (p.Val1740=) | single nucleotide variant | not provided [RCV001395455] | Chr9:114309262 [GRCh38] Chr9:117071542 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.62+4A>G | single nucleotide variant | Steel syndrome [RCV001332722] | Chr9:114156016 [GRCh38] Chr9:116918296 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1182T>C (p.Ser394=) | single nucleotide variant | not provided [RCV001494888] | Chr9:114168737 [GRCh38] Chr9:116931017 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4230G>A (p.Lys1410=) | single nucleotide variant | not provided [RCV001396088] | Chr9:114290081 [GRCh38] Chr9:117052361 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4008C>A (p.Gly1336=) | single nucleotide variant | not provided [RCV001502172] | Chr9:114288475 [GRCh38] Chr9:117050755 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3610-2A>G | single nucleotide variant | not provided [RCV001377546] | Chr9:114275659 [GRCh38] Chr9:117037939 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3248del (p.Lys1083fs) | deletion | not provided [RCV001387058] | Chr9:114264406 [GRCh38] Chr9:117026686 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.180G>A (p.Gly60=) | single nucleotide variant | not provided [RCV001453546] | Chr9:114167735 [GRCh38] Chr9:116930015 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.957A>G (p.Gln319=) | single nucleotide variant | not provided [RCV001492170] | Chr9:114168512 [GRCh38] Chr9:116930792 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3880-6T>C | single nucleotide variant | not provided [RCV001494597] | Chr9:114283703 [GRCh38] Chr9:117045983 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5526T>G (p.Pro1842=) | single nucleotide variant | not provided [RCV001495078] | Chr9:114310638 [GRCh38] Chr9:117072918 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.989G>A (p.Ser330Asn) | single nucleotide variant | not provided [RCV001450353] | Chr9:114168544 [GRCh38] Chr9:116930824 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1784C>T (p.Ala595Val) | single nucleotide variant | Inborn genetic diseases [RCV002562684]|not provided [RCV001482329] | Chr9:114169339 [GRCh38] Chr9:116931619 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.5307C>T (p.Asn1769=) | single nucleotide variant | not provided [RCV001485477] | Chr9:114309349 [GRCh38] Chr9:117071629 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.45G>A (p.Ala15=) | single nucleotide variant | not provided [RCV001485499] | Chr9:114155995 [GRCh38] Chr9:116918275 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3213C>T (p.Asp1071=) | single nucleotide variant | not provided [RCV001441023] | Chr9:114264372 [GRCh38] Chr9:117026652 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4719C>T (p.Val1573=) | single nucleotide variant | not provided [RCV001466696] | Chr9:114301089 [GRCh38] Chr9:117063369 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1413G>T (p.Pro471=) | single nucleotide variant | not provided [RCV001484077] | Chr9:114168968 [GRCh38] Chr9:116931248 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4296G>A (p.Val1432=) | single nucleotide variant | not provided [RCV001470010] | Chr9:114290259 [GRCh38] Chr9:117052539 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2031C>T (p.Asp677=) | single nucleotide variant | not provided [RCV001473263] | Chr9:114194418 [GRCh38] Chr9:116956698 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2601C>T (p.Pro867=) | single nucleotide variant | not provided [RCV001475091] | Chr9:114235634 [GRCh38] Chr9:116997914 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3837C>G (p.Gly1279=) | single nucleotide variant | not provided [RCV001482399] | Chr9:114282522 [GRCh38] Chr9:117044802 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.787G>A (p.Asp263Asn) | single nucleotide variant | Inborn genetic diseases [RCV002555580]|not provided [RCV001441262] | Chr9:114168342 [GRCh38] Chr9:116930622 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.1857T>C (p.Pro619=) | single nucleotide variant | not provided [RCV001435639] | Chr9:114169412 [GRCh38] Chr9:116931692 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4939-10C>T | single nucleotide variant | not provided [RCV001435710] | Chr9:114306510 [GRCh38] Chr9:117068790 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2646C>T (p.Pro882=) | single nucleotide variant | not provided [RCV001509790] | Chr9:114237007 [GRCh38] Chr9:116999287 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1707C>T (p.Ser569=) | single nucleotide variant | not provided [RCV001451364] | Chr9:114169262 [GRCh38] Chr9:116931542 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4236G>A (p.Gly1412=) | single nucleotide variant | not provided [RCV001499583] | Chr9:114290087 [GRCh38] Chr9:117052367 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2073T>C (p.Gly691=) | single nucleotide variant | not provided [RCV001485786] | Chr9:114195961 [GRCh38] Chr9:116958241 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3495G>A (p.Gly1165=) | single nucleotide variant | not provided [RCV001468593] | Chr9:114267551 [GRCh38] Chr9:117029831 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3473C>T (p.Pro1158Leu) | single nucleotide variant | not provided [RCV001417134] | Chr9:114267529 [GRCh38] Chr9:117029809 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2781+9del | deletion | not provided [RCV001464681] | Chr9:114240281 [GRCh38] Chr9:117002561 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3555+9_3555+20del | deletion | not provided [RCV001484520] | Chr9:114269303..114269314 [GRCh38] Chr9:117031583..117031594 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3525T>C (p.Thr1175=) | single nucleotide variant | not provided [RCV001470381] | Chr9:114269264 [GRCh38] Chr9:117031544 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2532C>T (p.Gly844=) | single nucleotide variant | not provided [RCV001479666] | Chr9:114231833 [GRCh38] Chr9:116994113 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5154C>T (p.Ile1718=) | single nucleotide variant | not provided [RCV001516111] | Chr9:114307715 [GRCh38] Chr9:117069995 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3630G>A (p.Gly1210=) | single nucleotide variant | not provided [RCV001502981] | Chr9:114275681 [GRCh38] Chr9:117037961 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1587T>A (p.Ala529=) | single nucleotide variant | not provided [RCV001482932] | Chr9:114169142 [GRCh38] Chr9:116931422 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1143C>T (p.Pro381=) | single nucleotide variant | not provided [RCV001476095] | Chr9:114168698 [GRCh38] Chr9:116930978 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3231A>G (p.Gln1077=) | single nucleotide variant | not provided [RCV001425018] | Chr9:114264390 [GRCh38] Chr9:117026670 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2250C>T (p.Pro750=) | single nucleotide variant | not provided [RCV001470804] | Chr9:114206278 [GRCh38] Chr9:116968558 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.666G>A (p.Thr222=) | single nucleotide variant | not provided [RCV001470886] | Chr9:114168221 [GRCh38] Chr9:116930501 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3147T>C (p.Pro1049=) | single nucleotide variant | not provided [RCV001473862] | Chr9:114258546 [GRCh38] Chr9:117020826 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-3dup | duplication | not provided [RCV001491139] | Chr9:114290215..114290216 [GRCh38] Chr9:117052495..117052496 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3502-4C>G | single nucleotide variant | not provided [RCV001458883] | Chr9:114269237 [GRCh38] Chr9:117031517 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2136C>T (p.Gly712=) | single nucleotide variant | not provided [RCV001458941] | Chr9:114205113 [GRCh38] Chr9:116967393 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5481C>A (p.Thr1827=) | single nucleotide variant | not provided [RCV001455350] | Chr9:114310593 [GRCh38] Chr9:117072873 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.522C>T (p.Cys174=) | single nucleotide variant | not provided [RCV001483123] | Chr9:114168077 [GRCh38] Chr9:116930357 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2175G>A (p.Gln725=) | single nucleotide variant | not provided [RCV001465163] | Chr9:114205764 [GRCh38] Chr9:116968044 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3780G>A (p.Lys1260=) | single nucleotide variant | not provided [RCV001473975] | Chr9:114282465 [GRCh38] Chr9:117044745 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2120G>A (p.Arg707Gln) | single nucleotide variant | not provided [RCV001516792] | Chr9:114196008 [GRCh38] Chr9:116958288 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3567C>A (p.Gly1189=) | single nucleotide variant | not provided [RCV001436602] | Chr9:114270739 [GRCh38] Chr9:117033019 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3502-5C>T | single nucleotide variant | not provided [RCV001467752] | Chr9:114269236 [GRCh38] Chr9:117031516 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5523C>T (p.Leu1841=) | single nucleotide variant | not provided [RCV001491276] | Chr9:114310635 [GRCh38] Chr9:117072915 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1200C>T (p.Ala400=) | single nucleotide variant | not provided [RCV001466077] | Chr9:114168755 [GRCh38] Chr9:116931035 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1794G>A (p.Leu598=) | single nucleotide variant | not provided [RCV001479323] | Chr9:114169349 [GRCh38] Chr9:116931629 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3718-6C>T | single nucleotide variant | not provided [RCV001491519] | Chr9:114282271 [GRCh38] Chr9:117044551 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4477-7C>T | single nucleotide variant | not provided [RCV001491550] | Chr9:114292096 [GRCh38] Chr9:117054376 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.819C>T (p.Thr273=) | single nucleotide variant | not provided [RCV001474338] | Chr9:114168374 [GRCh38] Chr9:116930654 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1119G>A (p.Ser373=) | single nucleotide variant | not provided [RCV001452543] | Chr9:114168674 [GRCh38] Chr9:116930954 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.27C>G (p.Ala9=) | single nucleotide variant | not provided [RCV001503933] | Chr9:114155977 [GRCh38] Chr9:116918257 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4092G>C (p.Gly1364=) | single nucleotide variant | not provided [RCV001459741] | Chr9:114288749 [GRCh38] Chr9:117051029 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5107+10C>T | single nucleotide variant | not provided [RCV001400491] | Chr9:114306698 [GRCh38] Chr9:117068978 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.62+7A>G | single nucleotide variant | not provided [RCV001405692] | Chr9:114156019 [GRCh38] Chr9:116918299 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4092G>A (p.Gly1364=) | single nucleotide variant | not provided [RCV001499729] | Chr9:114288749 [GRCh38] Chr9:117051029 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3879+7A>G | single nucleotide variant | not provided [RCV001455607] | Chr9:114282571 [GRCh38] Chr9:117044851 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4287G>A (p.Arg1429=) | single nucleotide variant | not provided [RCV001471755] | Chr9:114290250 [GRCh38] Chr9:117052530 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3378C>A (p.Gly1126=) | single nucleotide variant | not provided [RCV001489089] | Chr9:114265460 [GRCh38] Chr9:117027740 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.722C>T (p.Thr241Met) | single nucleotide variant | Inborn genetic diseases [RCV002561998]|not provided [RCV001477306] | Chr9:114168277 [GRCh38] Chr9:116930557 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.475C>T (p.Leu159=) | single nucleotide variant | not provided [RCV001477326] | Chr9:114168030 [GRCh38] Chr9:116930310 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3282G>A (p.Arg1094=) | single nucleotide variant | not provided [RCV001477444] | Chr9:114264956 [GRCh38] Chr9:117027236 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1159C>A (p.Pro387Thr) | single nucleotide variant | not provided [RCV001500970] | Chr9:114168714 [GRCh38] Chr9:116930994 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5421_5422inv (p.Met1808Val) | inversion | not provided [RCV001418469] | Chr9:114309463..114309464 [GRCh38] Chr9:117071743..117071744 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3567C>G (p.Gly1189=) | single nucleotide variant | not provided [RCV001439638] | Chr9:114270739 [GRCh38] Chr9:117033019 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.102T>C (p.Cys34=) | single nucleotide variant | not provided [RCV001442381] | Chr9:114162754 [GRCh38] Chr9:116925034 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3576T>C (p.Gly1192=) | single nucleotide variant | not provided [RCV001521331] | Chr9:114270748 [GRCh38] Chr9:117033028 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4702-7C>G | single nucleotide variant | not provided [RCV001489336] | Chr9:114301065 [GRCh38] Chr9:117063345 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4644G>A (p.Pro1548=) | single nucleotide variant | not provided [RCV001398013] | Chr9:114300630 [GRCh38] Chr9:117062910 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5218-8C>A | single nucleotide variant | not provided [RCV001463208] | Chr9:114309252 [GRCh38] Chr9:117071532 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1932A>G (p.Leu644=) | single nucleotide variant | not provided [RCV001521615] | Chr9:114178314 [GRCh38] Chr9:116940594 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.441C>T (p.Phe147=) | single nucleotide variant | not provided [RCV001489455] | Chr9:114167996 [GRCh38] Chr9:116930276 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4824C>T (p.Pro1608=) | single nucleotide variant | not provided [RCV001491747] | Chr9:114301696 [GRCh38] Chr9:117063976 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4479T>A (p.Gly1493=) | single nucleotide variant | not provided [RCV001463838] | Chr9:114292105 [GRCh38] Chr9:117054385 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1998C>T (p.Pro666=) | single nucleotide variant | not provided [RCV001484372] | Chr9:114183057 [GRCh38] Chr9:116945337 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4494C>T (p.Pro1498=) | single nucleotide variant | not provided [RCV001467134] | Chr9:114292120 [GRCh38] Chr9:117054400 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.186T>C (p.Pro62=) | single nucleotide variant | not provided [RCV001426625] | Chr9:114167741 [GRCh38] Chr9:116930021 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3210G>A (p.Pro1070=) | single nucleotide variant | not provided [RCV001442637] | Chr9:114264369 [GRCh38] Chr9:117026649 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.63-9G>C | single nucleotide variant | not provided [RCV001493178] | Chr9:114162706 [GRCh38] Chr9:116924986 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4792-8C>T | single nucleotide variant | not provided [RCV001467313] | Chr9:114301437 [GRCh38] Chr9:117063717 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1302G>A (p.Arg434=) | single nucleotide variant | not provided [RCV001463587] | Chr9:114168857 [GRCh38] Chr9:116931137 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2508C>T (p.Pro836=) | single nucleotide variant | not provided [RCV001466457] | Chr9:114231120 [GRCh38] Chr9:116993400 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1065A>G (p.Pro355=) | single nucleotide variant | not provided [RCV001466473] | Chr9:114168620 [GRCh38] Chr9:116930900 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3534G>A (p.Glu1178=) | single nucleotide variant | not provided [RCV001491936] | Chr9:114269273 [GRCh38] Chr9:117031553 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.171G>A (p.Thr57=) | single nucleotide variant | not provided [RCV001464210] | Chr9:114167726 [GRCh38] Chr9:116930006 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2097C>T (p.Ser699=) | single nucleotide variant | not provided [RCV001484838] | Chr9:114195985 [GRCh38] Chr9:116958265 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1216C>T (p.Gln406Ter) | single nucleotide variant | Steel syndrome [RCV002499806]|not provided [RCV001386749] | Chr9:114168771 [GRCh38] Chr9:116931051 [GRCh37] Chr9:9q32 |
pathogenic|likely pathogenic |
NM_032888.4(COL27A1):c.312C>G (p.Leu104=) | single nucleotide variant | not provided [RCV001442923] | Chr9:114167867 [GRCh38] Chr9:116930147 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5265A>G (p.Leu1755=) | single nucleotide variant | not provided [RCV001474788] | Chr9:114309307 [GRCh38] Chr9:117071587 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4800A>G (p.Gln1600=) | single nucleotide variant | not provided [RCV001453991] | Chr9:114301453 [GRCh38] Chr9:117063733 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.903A>G (p.Gln301=) | single nucleotide variant | not provided [RCV001457133] | Chr9:114168458 [GRCh38] Chr9:116930738 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-9G>T | single nucleotide variant | not provided [RCV001497780] | Chr9:114250606 [GRCh38] Chr9:117012886 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1365C>A (p.Pro455=) | single nucleotide variant | COL27A1-related condition [RCV003938756]|not provided [RCV001435069] | Chr9:114168920 [GRCh38] Chr9:116931200 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2797C>T (p.Arg933Ter) | single nucleotide variant | not provided [RCV001384340] | Chr9:114240449 [GRCh38] Chr9:117002729 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.60G>C (p.Gly20=) | single nucleotide variant | not provided [RCV001471590] | Chr9:114156010 [GRCh38] Chr9:116918290 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3033+7G>A | single nucleotide variant | not provided [RCV001435251] | Chr9:114250675 [GRCh38] Chr9:117012955 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.699G>A (p.Arg233=) | single nucleotide variant | not provided [RCV001419562] | Chr9:114168254 [GRCh38] Chr9:116930534 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3195+8G>T | single nucleotide variant | not provided [RCV001429879] | Chr9:114258602 [GRCh38] Chr9:117020882 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4939-7G>A | single nucleotide variant | COL27A1-related condition [RCV003908611]|not provided [RCV001418404] | Chr9:114306513 [GRCh38] Chr9:117068793 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2055C>A (p.Ala685=) | single nucleotide variant | not provided [RCV001406632] | Chr9:114194442 [GRCh38] Chr9:116956722 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1908+7C>T | single nucleotide variant | not provided [RCV001445929] | Chr9:114169470 [GRCh38] Chr9:116931750 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1155C>T (p.Pro385=) | single nucleotide variant | not provided [RCV001437093] | Chr9:114168710 [GRCh38] Chr9:116930990 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1641C>T (p.Pro547=) | single nucleotide variant | not provided [RCV001419930] | Chr9:114169196 [GRCh38] Chr9:116931476 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2805G>A (p.Leu935=) | single nucleotide variant | not provided [RCV001409347] | Chr9:114240457 [GRCh38] Chr9:117002737 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4311C>G (p.Leu1437=) | single nucleotide variant | not provided [RCV001417232] | Chr9:114290274 [GRCh38] Chr9:117052554 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2472C>T (p.Asp824=) | single nucleotide variant | not provided [RCV001443817] | Chr9:114231084 [GRCh38] Chr9:116993364 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1026C>T (p.Gly342=) | single nucleotide variant | not provided [RCV001409639] | Chr9:114168581 [GRCh38] Chr9:116930861 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4383C>T (p.Asp1461=) | single nucleotide variant | not provided [RCV001394289] | Chr9:114290824 [GRCh38] Chr9:117053104 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-5C>T | single nucleotide variant | not provided [RCV001428845] | Chr9:114290219 [GRCh38] Chr9:117052499 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.249G>A (p.Gln83=) | single nucleotide variant | not provided [RCV001448857] | Chr9:114167804 [GRCh38] Chr9:116930084 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3365dup (p.Gly1123fs) | duplication | not provided [RCV001385242] | Chr9:114265441..114265442 [GRCh38] Chr9:117027721..117027722 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2323-6C>T | single nucleotide variant | not provided [RCV001415567] | Chr9:114210976 [GRCh38] Chr9:116973256 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4254G>T (p.Gly1418=) | single nucleotide variant | not provided [RCV001427935] | Chr9:114290105 [GRCh38] Chr9:117052385 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3501+9G>C | single nucleotide variant | not provided [RCV001430243] | Chr9:114267566 [GRCh38] Chr9:117029846 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3459T>C (p.Gly1153=) | single nucleotide variant | not provided [RCV001409716] | Chr9:114267515 [GRCh38] Chr9:117029795 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2521-2A>C | single nucleotide variant | not provided [RCV001378441] | Chr9:114231820 [GRCh38] Chr9:116994100 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2269-9C>G | single nucleotide variant | not provided [RCV001407489] | Chr9:114209666 [GRCh38] Chr9:116971946 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5217+9C>T | single nucleotide variant | not provided [RCV001446717] | Chr9:114307787 [GRCh38] Chr9:117070067 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-7C>T | single nucleotide variant | not provided [RCV001423537] | Chr9:114290217 [GRCh38] Chr9:117052497 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4080G>A (p.Pro1360=) | single nucleotide variant | not provided [RCV001393255] | Chr9:114288737 [GRCh38] Chr9:117051017 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3502-8del | deletion | not provided [RCV001437409] | Chr9:114269232 [GRCh38] Chr9:117031512 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2337T>C (p.Val779=) | single nucleotide variant | not provided [RCV001437444] | Chr9:114210996 [GRCh38] Chr9:116973276 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.697_707del (p.Arg233fs) | deletion | not provided [RCV001381319] | Chr9:114168250..114168260 [GRCh38] Chr9:116930530..116930540 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.5034G>C (p.Thr1678=) | single nucleotide variant | not provided [RCV001449056] | Chr9:114306615 [GRCh38] Chr9:117068895 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2169+7GCCTCA[3] | microsatellite | not provided [RCV001449090] | Chr9:114205152..114205153 [GRCh38] Chr9:116967432..116967433 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4686G>A (p.Gly1562=) | single nucleotide variant | not provided [RCV001449095] | Chr9:114300672 [GRCh38] Chr9:117062952 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.447C>T (p.Leu149=) | single nucleotide variant | not provided [RCV001400289] | Chr9:114168002 [GRCh38] Chr9:116930282 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4011G>A (p.Lys1337=) | single nucleotide variant | not provided [RCV001430805] | Chr9:114288478 [GRCh38] Chr9:117050758 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5160C>T (p.Val1720=) | single nucleotide variant | not provided [RCV001446858] | Chr9:114307721 [GRCh38] Chr9:117070001 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1608C>T (p.Pro536=) | single nucleotide variant | not provided [RCV001444140] | Chr9:114169163 [GRCh38] Chr9:116931443 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4792-10C>T | single nucleotide variant | not provided [RCV001410019] | Chr9:114301435 [GRCh38] Chr9:117063715 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4683G>A (p.Arg1561=) | single nucleotide variant | not provided [RCV001446746] | Chr9:114300669 [GRCh38] Chr9:117062949 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3092A>G (p.His1031Arg) | single nucleotide variant | Inborn genetic diseases [RCV002560326]|not provided [RCV001449243] | Chr9:114252883 [GRCh38] Chr9:117015163 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.2763T>C (p.Asn921=) | single nucleotide variant | not provided [RCV001449354] | Chr9:114240255 [GRCh38] Chr9:117002535 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3191G>A (p.Arg1064His) | single nucleotide variant | not provided [RCV001430967] | Chr9:114258590 [GRCh38] Chr9:117020870 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2343C>A (p.Gly781=) | single nucleotide variant | not provided [RCV001447046] | Chr9:114211002 [GRCh38] Chr9:116973282 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1833C>T (p.Ile611=) | single nucleotide variant | not provided [RCV001415823] | Chr9:114169388 [GRCh38] Chr9:116931668 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2125-9C>T | single nucleotide variant | not provided [RCV001428065] | Chr9:114205093 [GRCh38] Chr9:116967373 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.99C>T (p.Ala33=) | single nucleotide variant | not provided [RCV001430689] | Chr9:114162751 [GRCh38] Chr9:116925031 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2694A>C (p.Gly898=) | single nucleotide variant | not provided [RCV001441592] | Chr9:114237682 [GRCh38] Chr9:116999962 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2064G>A (p.Gly688=) | single nucleotide variant | not provided [RCV001449468] | Chr9:114194451 [GRCh38] Chr9:116956731 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4846-2A>G | single nucleotide variant | not provided [RCV001378856] | Chr9:114302080 [GRCh38] Chr9:117064360 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2667G>A (p.Gly889=) | single nucleotide variant | not provided [RCV001418221] | Chr9:114237028 [GRCh38] Chr9:116999308 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1263C>T (p.Pro421=) | single nucleotide variant | not provided [RCV001410554] | Chr9:114168818 [GRCh38] Chr9:116931098 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2808G>A (p.Pro936=) | single nucleotide variant | not provided [RCV001398172] | Chr9:114240460 [GRCh38] Chr9:117002740 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2007T>G (p.Pro669=) | single nucleotide variant | not provided [RCV001405316] | Chr9:114183066 [GRCh38] Chr9:116945346 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.915C>T (p.Pro305=) | single nucleotide variant | not provided [RCV001431198] | Chr9:114168470 [GRCh38] Chr9:116930750 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3518_3519insAGGG (p.Thr1175fs) | insertion | not provided [RCV001386618] | Chr9:114269257..114269258 [GRCh38] Chr9:117031537..117031538 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1635C>T (p.Ala545=) | single nucleotide variant | not provided [RCV001410567] | Chr9:114169190 [GRCh38] Chr9:116931470 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1170A>G (p.Lys390=) | single nucleotide variant | not provided [RCV001408366] | Chr9:114168725 [GRCh38] Chr9:116931005 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.723G>A (p.Thr241=) | single nucleotide variant | not provided [RCV001437810] | Chr9:114168278 [GRCh38] Chr9:116930558 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4369-2_4369-1del | deletion | not provided [RCV001379663] | Chr9:114290808..114290809 [GRCh38] Chr9:117053088..117053089 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.564C>T (p.Asp188=) | single nucleotide variant | not provided [RCV001408115] | Chr9:114168119 [GRCh38] Chr9:116930399 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1713G>A (p.Leu571=) | single nucleotide variant | not provided [RCV001423541] | Chr9:114169268 [GRCh38] Chr9:116931548 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4716C>T (p.Ile1572=) | single nucleotide variant | not provided [RCV001426731] | Chr9:114301086 [GRCh38] Chr9:117063366 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2835+10T>G | single nucleotide variant | not provided [RCV001410917] | Chr9:114240497 [GRCh38] Chr9:117002777 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.63-1G>A | single nucleotide variant | not provided [RCV001377137] | Chr9:114162714 [GRCh38] Chr9:116924994 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3276G>T (p.Pro1092=) | single nucleotide variant | not provided [RCV001417705] | Chr9:114264950 [GRCh38] Chr9:117027230 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4020G>C (p.Gly1340=) | single nucleotide variant | not provided [RCV001398241] | Chr9:114288487 [GRCh38] Chr9:117050767 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4152+1G>A | single nucleotide variant | not provided [RCV001377177] | Chr9:114288968 [GRCh38] Chr9:117051248 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.702G>A (p.Lys234=) | single nucleotide variant | not provided [RCV001393651] | Chr9:114168257 [GRCh38] Chr9:116930537 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3915G>A (p.Pro1305=) | single nucleotide variant | not provided [RCV001431509] | Chr9:114283744 [GRCh38] Chr9:117046024 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2961G>A (p.Pro987=) | single nucleotide variant | not provided [RCV001411005] | Chr9:114245892 [GRCh38] Chr9:117008172 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4153-4G>C | single nucleotide variant | not provided [RCV001408521] | Chr9:114289238 [GRCh38] Chr9:117051518 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3327G>A (p.Ser1109=) | single nucleotide variant | not provided [RCV001416304] | Chr9:114265098 [GRCh38] Chr9:117027378 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4311C>T (p.Leu1437=) | single nucleotide variant | not provided [RCV001445452] | Chr9:114290274 [GRCh38] Chr9:117052554 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5271C>T (p.Ser1757=) | single nucleotide variant | not provided [RCV001445459] | Chr9:114309313 [GRCh38] Chr9:117071593 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3669G>A (p.Leu1223=) | single nucleotide variant | not provided [RCV001418089] | Chr9:114275720 [GRCh38] Chr9:117038000 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4584+8A>G | single nucleotide variant | not provided [RCV001406154] | Chr9:114292218 [GRCh38] Chr9:117054498 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.961C>T (p.Pro321Ser) | single nucleotide variant | Inborn genetic diseases [RCV002555595]|not provided [RCV001442690] | Chr9:114168516 [GRCh38] Chr9:116930796 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.3810C>T (p.Gly1270=) | single nucleotide variant | not provided [RCV001445403] | Chr9:114282495 [GRCh38] Chr9:117044775 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2269-8T>C | single nucleotide variant | not provided [RCV001435146] | Chr9:114209667 [GRCh38] Chr9:116971947 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4701+7T>C | single nucleotide variant | not provided [RCV001427260] | Chr9:114300694 [GRCh38] Chr9:117062974 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1854G>T (p.Thr618=) | single nucleotide variant | not provided [RCV001427265] | Chr9:114169409 [GRCh38] Chr9:116931689 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.51G>C (p.Ala17=) | single nucleotide variant | not provided [RCV001401685] | Chr9:114156001 [GRCh38] Chr9:116918281 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1566C>T (p.Ala522=) | single nucleotide variant | not provided [RCV001440464] | Chr9:114169121 [GRCh38] Chr9:116931401 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.24G>C (p.Gly8=) | single nucleotide variant | not provided [RCV001440503] | Chr9:114155974 [GRCh38] Chr9:116918254 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4863T>C (p.Pro1621=) | single nucleotide variant | not provided [RCV001445622] | Chr9:114302099 [GRCh38] Chr9:117064379 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.705G>A (p.Gln235=) | single nucleotide variant | not provided [RCV001435220] | Chr9:114168260 [GRCh38] Chr9:116930540 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4873-8T>G | single nucleotide variant | not provided [RCV001411516] | Chr9:114304600 [GRCh38] Chr9:117066880 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2925T>C (p.Asp975=) | single nucleotide variant | not provided [RCV001409147] | Chr9:114243551 [GRCh38] Chr9:117005831 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5289C>T (p.Ile1763=) | single nucleotide variant | not provided [RCV001409179] | Chr9:114309331 [GRCh38] Chr9:117071611 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4833G>T (p.Arg1611=) | single nucleotide variant | not provided [RCV001427512] | Chr9:114301705 [GRCh38] Chr9:117063985 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.665C>T (p.Thr222Met) | single nucleotide variant | not provided [RCV001409141] | Chr9:114168220 [GRCh38] Chr9:116930500 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2323-9C>T | single nucleotide variant | not provided [RCV001409324] | Chr9:114210973 [GRCh38] Chr9:116973253 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5190G>T (p.Thr1730=) | single nucleotide variant | not provided [RCV001448574] | Chr9:114307751 [GRCh38] Chr9:117070031 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4017G>A (p.Glu1339=) | single nucleotide variant | not provided [RCV001495134] | Chr9:114288484 [GRCh38] Chr9:117050764 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2982A>T (p.Gly994=) | single nucleotide variant | not provided [RCV001478850] | Chr9:114250617 [GRCh38] Chr9:117012897 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4140G>A (p.Gln1380=) | single nucleotide variant | not provided [RCV001482012] | Chr9:114288955 [GRCh38] Chr9:117051235 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1504C>A (p.Arg502=) | single nucleotide variant | not provided [RCV001495133] | Chr9:114169059 [GRCh38] Chr9:116931339 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1839C>T (p.His613=) | single nucleotide variant | not provided [RCV001472622] | Chr9:114169394 [GRCh38] Chr9:116931674 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.873T>C (p.Thr291=) | single nucleotide variant | not provided [RCV001478747] | Chr9:114168428 [GRCh38] Chr9:116930708 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5218-6C>T | single nucleotide variant | not provided [RCV001457166] | Chr9:114309254 [GRCh38] Chr9:117071534 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3262C>A (p.Pro1088Thr) | single nucleotide variant | not provided [RCV001479118] | Chr9:114264936 [GRCh38] Chr9:117027216 [GRCh37] Chr9:9q32 |
likely benign|conflicting interpretations of pathogenicity |
NM_032888.4(COL27A1):c.2712G>A (p.Gly904=) | single nucleotide variant | not provided [RCV001450784] | Chr9:114237700 [GRCh38] Chr9:116999980 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.345C>T (p.Phe115=) | single nucleotide variant | not provided [RCV001481959] | Chr9:114167900 [GRCh38] Chr9:116930180 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4488G>A (p.Gly1496=) | single nucleotide variant | not provided [RCV001465182] | Chr9:114292114 [GRCh38] Chr9:117054394 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2427A>G (p.Glu809=) | single nucleotide variant | not provided [RCV001482524] | Chr9:114222228 [GRCh38] Chr9:116984508 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2160C>T (p.Pro720=) | single nucleotide variant | not provided [RCV001457812] | Chr9:114205137 [GRCh38] Chr9:116967417 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1785G>A (p.Ala595=) | single nucleotide variant | not provided [RCV001476073] | Chr9:114169340 [GRCh38] Chr9:116931620 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4043G>A (p.Arg1348Gln) | single nucleotide variant | not provided [RCV001510367] | Chr9:114288510 [GRCh38] Chr9:117050790 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4107G>A (p.Glu1369=) | single nucleotide variant | not provided [RCV001510368] | Chr9:114288922 [GRCh38] Chr9:117051202 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1095C>T (p.Pro365=) | single nucleotide variant | not provided [RCV001458828] | Chr9:114168650 [GRCh38] Chr9:116930930 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2016+10T>C | single nucleotide variant | not provided [RCV001465606] | Chr9:114183085 [GRCh38] Chr9:116945365 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3324C>T (p.Gly1108=) | single nucleotide variant | not provided [RCV001473968] | Chr9:114265095 [GRCh38] Chr9:117027375 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4470A>G (p.Gly1490=) | single nucleotide variant | not provided [RCV001473984] | Chr9:114290911 [GRCh38] Chr9:117053191 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.932A>G (p.His311Arg) | single nucleotide variant | not provided [RCV001502849] | Chr9:114168487 [GRCh38] Chr9:116930767 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5568T>C (p.Pro1856=) | single nucleotide variant | not provided [RCV001479867] | Chr9:114310680 [GRCh38] Chr9:117072960 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3347C>A (p.Pro1116Gln) | single nucleotide variant | not provided [RCV001510897] | Chr9:114265429 [GRCh38] Chr9:117027709 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2482T>C (p.Leu828=) | single nucleotide variant | COL27A1-related condition [RCV003948437]|not provided [RCV001491445] | Chr9:114231094 [GRCh38] Chr9:116993374 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4407C>T (p.Gly1469=) | single nucleotide variant | not provided [RCV001496865] | Chr9:114290848 [GRCh38] Chr9:117053128 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4947C>T (p.Ser1649=) | single nucleotide variant | not provided [RCV001486825] | Chr9:114306528 [GRCh38] Chr9:117068808 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3201C>G (p.Pro1067=) | single nucleotide variant | not provided [RCV001486934] | Chr9:114264360 [GRCh38] Chr9:117026640 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2562T>C (p.Asp854=) | single nucleotide variant | not provided [RCV001462483] | Chr9:114231863 [GRCh38] Chr9:116994143 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4045-6A>T | single nucleotide variant | not provided [RCV001455648] | Chr9:114288696 [GRCh38] Chr9:117050976 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.428G>A (p.Arg143His) | single nucleotide variant | not provided [RCV001466249] | Chr9:114167983 [GRCh38] Chr9:116930263 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4810-10G>T | single nucleotide variant | not provided [RCV001500219] | Chr9:114301672 [GRCh38] Chr9:117063952 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3786T>C (p.Tyr1262=) | single nucleotide variant | Steel syndrome [RCV001543914]|not provided [RCV001512063] | Chr9:114282471 [GRCh38] Chr9:117044751 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3303T>G (p.Ala1101=) | single nucleotide variant | not provided [RCV001470295] | Chr9:114265074 [GRCh38] Chr9:117027354 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.796C>T (p.Leu266=) | single nucleotide variant | not provided [RCV001452186] | Chr9:114168351 [GRCh38] Chr9:116930631 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1560A>G (p.Ala520=) | single nucleotide variant | not provided [RCV001480189] | Chr9:114169115 [GRCh38] Chr9:116931395 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4398C>A (p.Gly1466=) | single nucleotide variant | not provided [RCV001480557] | Chr9:114290839 [GRCh38] Chr9:117053119 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4173G>A (p.Gly1391=) | single nucleotide variant | not provided [RCV001463317] | Chr9:114289262 [GRCh38] Chr9:117051542 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5238G>C (p.Arg1746=) | single nucleotide variant | not provided [RCV001456133] | Chr9:114309280 [GRCh38] Chr9:117071560 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4078C>A (p.Pro1360Thr) | single nucleotide variant | Inborn genetic diseases [RCV002561997]|not provided [RCV001477301] | Chr9:114288735 [GRCh38] Chr9:117051015 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.5208G>A (p.Thr1736=) | single nucleotide variant | not provided [RCV001497245] | Chr9:114307769 [GRCh38] Chr9:117070049 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3888G>A (p.Pro1296=) | single nucleotide variant | not provided [RCV001512764] | Chr9:114283717 [GRCh38] Chr9:117045997 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1287C>T (p.Asn429=) | single nucleotide variant | not provided [RCV001480746] | Chr9:114168842 [GRCh38] Chr9:116931122 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3609+9C>G | single nucleotide variant | not provided [RCV001466765] | Chr9:114270790 [GRCh38] Chr9:117033070 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5418G>A (p.Val1806=) | single nucleotide variant | not provided [RCV001460229] | Chr9:114309460 [GRCh38] Chr9:117071740 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.396C>T (p.Pro132=) | single nucleotide variant | not provided [RCV001453037] | Chr9:114167951 [GRCh38] Chr9:116930231 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4746G>A (p.Ser1582=) | single nucleotide variant | not provided [RCV001518099] | Chr9:114301116 [GRCh38] Chr9:117063396 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.165C>T (p.Ser55=) | single nucleotide variant | not provided [RCV001463767] | Chr9:114167720 [GRCh38] Chr9:116930000 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1056C>T (p.Ala352=) | single nucleotide variant | not provided [RCV001460446] | Chr9:114168611 [GRCh38] Chr9:116930891 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3189A>T (p.Gly1063=) | single nucleotide variant | not provided [RCV001504737] | Chr9:114258588 [GRCh38] Chr9:117020868 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3756C>A (p.Gly1252=) | single nucleotide variant | not provided [RCV001460692] | Chr9:114282315 [GRCh38] Chr9:117044595 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2145A>G (p.Gly715=) | single nucleotide variant | not provided [RCV001471409] | Chr9:114205122 [GRCh38] Chr9:116967402 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3609+10C>T | single nucleotide variant | not provided [RCV001501098] | Chr9:114270791 [GRCh38] Chr9:117033071 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4662C>T (p.Phe1554=) | single nucleotide variant | not provided [RCV001463688] | Chr9:114300648 [GRCh38] Chr9:117062928 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1359C>T (p.Pro453=) | single nucleotide variant | not provided [RCV001463749] | Chr9:114168914 [GRCh38] Chr9:116931194 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2928C>T (p.Gly976=) | single nucleotide variant | not provided [RCV001501340] | Chr9:114243554 [GRCh38] Chr9:117005834 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4083A>G (p.Gly1361=) | single nucleotide variant | Steel syndrome [RCV001543917]|not provided [RCV001514502] | Chr9:114288740 [GRCh38] Chr9:117051020 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.5422A>G (p.Met1808Val) | single nucleotide variant | not provided [RCV001514503] | Chr9:114309464 [GRCh38] Chr9:117071744 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3681C>T (p.Asp1227=) | single nucleotide variant | not provided [RCV001505101] | Chr9:114275732 [GRCh38] Chr9:117038012 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4194G>A (p.Ser1398=) | single nucleotide variant | not provided [RCV001472161] | Chr9:114289283 [GRCh38] Chr9:117051563 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2490G>A (p.Pro830=) | single nucleotide variant | not provided [RCV001498500] | Chr9:114231102 [GRCh38] Chr9:116993382 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3972A>C (p.Gly1324=) | single nucleotide variant | not provided [RCV001478687] | Chr9:114284762 [GRCh38] Chr9:117047042 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.177C>T (p.Ala59=) | single nucleotide variant | not provided [RCV001464445] | Chr9:114167732 [GRCh38] Chr9:116930012 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5034G>T (p.Thr1678=) | single nucleotide variant | not provided [RCV001425283] | Chr9:114306615 [GRCh38] Chr9:117068895 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3327G>C (p.Ser1109=) | single nucleotide variant | not provided [RCV001462423] | Chr9:114265098 [GRCh38] Chr9:117027378 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4374G>A (p.Glu1458=) | single nucleotide variant | not provided [RCV001499867] | Chr9:114290815 [GRCh38] Chr9:117053095 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4968G>A (p.Leu1656=) | single nucleotide variant | not provided [RCV001468945] | Chr9:114306549 [GRCh38] Chr9:117068829 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4792-5T>G | single nucleotide variant | not provided [RCV001469567] | Chr9:114301440 [GRCh38] Chr9:117063720 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1502C>T (p.Thr501Ile) | single nucleotide variant | not provided [RCV001472895] | Chr9:114169057 [GRCh38] Chr9:116931337 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2841T>C (p.Asp947=) | single nucleotide variant | not provided [RCV001399390] | Chr9:114242192 [GRCh38] Chr9:117004472 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2769A>G (p.Pro923=) | single nucleotide variant | not provided [RCV001462498] | Chr9:114240261 [GRCh38] Chr9:117002541 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1830G>A (p.Ser610=) | single nucleotide variant | not provided [RCV001479792] | Chr9:114169385 [GRCh38] Chr9:116931665 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2148G>A (p.Pro716=) | single nucleotide variant | not provided [RCV001465455] | Chr9:114205125 [GRCh38] Chr9:116967405 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2275A>C (p.Ile759Leu) | single nucleotide variant | not provided [RCV001467124] | Chr9:114209681 [GRCh38] Chr9:116971961 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.54G>A (p.Ala18=) | single nucleotide variant | not provided [RCV001485834] | Chr9:114156004 [GRCh38] Chr9:116918284 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3934-5T>C | single nucleotide variant | not provided [RCV001486224] | Chr9:114284719 [GRCh38] Chr9:117046999 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2881-7G>A | single nucleotide variant | not provided [RCV001469948] | Chr9:114243500 [GRCh38] Chr9:117005780 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2323-6del | deletion | not provided [RCV001487312] | Chr9:114210973 [GRCh38] Chr9:116973253 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5073G>A (p.Arg1691=) | single nucleotide variant | not provided [RCV001473418] | Chr9:114306654 [GRCh38] Chr9:117068934 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4905G>C (p.Thr1635=) | single nucleotide variant | not provided [RCV001450833] | Chr9:114304640 [GRCh38] Chr9:117066920 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.411C>A (p.Val137=) | single nucleotide variant | not provided [RCV001401615] | Chr9:114167966 [GRCh38] Chr9:116930246 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3627A>C (p.Pro1209=) | single nucleotide variant | not provided [RCV001428890] | Chr9:114275678 [GRCh38] Chr9:117037958 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4161G>A (p.Pro1387=) | single nucleotide variant | not provided [RCV001431401] | Chr9:114289250 [GRCh38] Chr9:117051530 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2334C>T (p.Gly778=) | single nucleotide variant | not provided [RCV001516501] | Chr9:114210993 [GRCh38] Chr9:116973273 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3120C>A (p.Thr1040=) | single nucleotide variant | not provided [RCV001498538] | Chr9:114252911 [GRCh38] Chr9:117015191 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2436G>A (p.Leu812=) | single nucleotide variant | not provided [RCV001428920] | Chr9:114222237 [GRCh38] Chr9:116984517 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3295-4C>G | single nucleotide variant | not provided [RCV001403513] | Chr9:114265062 [GRCh38] Chr9:117027342 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1831A>T (p.Ile611Phe) | single nucleotide variant | Steel syndrome [RCV001543750]|not provided [RCV001509917] | Chr9:114169386 [GRCh38] Chr9:116931666 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2620-7C>A | single nucleotide variant | not provided [RCV001460533] | Chr9:114236974 [GRCh38] Chr9:116999254 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1299C>T (p.Pro433=) | single nucleotide variant | not provided [RCV001500202] | Chr9:114168854 [GRCh38] Chr9:116931134 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4938+9A>C | single nucleotide variant | not provided [RCV001482091] | Chr9:114304682 [GRCh38] Chr9:117066962 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2142T>C (p.Pro714=) | single nucleotide variant | not provided [RCV001465653] | Chr9:114205119 [GRCh38] Chr9:116967399 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.144C>T (p.Ile48=) | single nucleotide variant | not provided [RCV001468678] | Chr9:114167699 [GRCh38] Chr9:116929979 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1040C>T (p.Thr347Met) | single nucleotide variant | not provided [RCV001491048] | Chr9:114168595 [GRCh38] Chr9:116930875 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3177G>A (p.Arg1059=) | single nucleotide variant | not provided [RCV001491126] | Chr9:114258576 [GRCh38] Chr9:117020856 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3088-5G>C | single nucleotide variant | not provided [RCV001491153] | Chr9:114252874 [GRCh38] Chr9:117015154 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1264G>A (p.Ala422Thr) | single nucleotide variant | Steel syndrome [RCV001543748]|not provided [RCV001512059] | Chr9:114168819 [GRCh38] Chr9:116931099 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2889T>G (p.Pro963=) | single nucleotide variant | not provided [RCV001497236] | Chr9:114243515 [GRCh38] Chr9:117005795 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4845+7A>G | single nucleotide variant | not provided [RCV001461128] | Chr9:114301724 [GRCh38] Chr9:117064004 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4854A>G (p.Pro1618=) | single nucleotide variant | not provided [RCV001453937] | Chr9:114302090 [GRCh38] Chr9:117064370 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5412C>T (p.Pro1804=) | single nucleotide variant | not provided [RCV001429203] | Chr9:114309454 [GRCh38] Chr9:117071734 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3088-4G>T | single nucleotide variant | not provided [RCV001475998] | Chr9:114252875 [GRCh38] Chr9:117015155 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2169+8C>T | single nucleotide variant | not provided [RCV001483072] | Chr9:114205154 [GRCh38] Chr9:116967434 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3951G>A (p.Val1317=) | single nucleotide variant | COL27A1-related condition [RCV003931032]|not provided [RCV001503335] | Chr9:114284741 [GRCh38] Chr9:117047021 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.5313C>T (p.Thr1771=) | single nucleotide variant | not provided [RCV001469472] | Chr9:114309355 [GRCh38] Chr9:117071635 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.93G>A (p.Ser31=) | single nucleotide variant | not provided [RCV001491464] | Chr9:114162745 [GRCh38] Chr9:116925025 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4810-10G>A | single nucleotide variant | not provided [RCV001440092] | Chr9:114301672 [GRCh38] Chr9:117063952 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5582G>A (p.Ter1861=) | single nucleotide variant | not provided [RCV001406270] | Chr9:114310694 [GRCh38] Chr9:117072974 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.570A>G (p.Ala190=) | single nucleotide variant | not provided [RCV001484823] | Chr9:114168125 [GRCh38] Chr9:116930405 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.963G>A (p.Pro321=) | single nucleotide variant | not provided [RCV001484824] | Chr9:114168518 [GRCh38] Chr9:116930798 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-3del | deletion | not provided [RCV001510912] | Chr9:114290216 [GRCh38] Chr9:117052496 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.105C>T (p.His35=) | single nucleotide variant | not provided [RCV001442900] | Chr9:114162757 [GRCh38] Chr9:116925037 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5430C>T (p.Gly1810=) | single nucleotide variant | not provided [RCV001510717] | Chr9:114309472 [GRCh38] Chr9:117071752 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.870G>A (p.Gly290=) | single nucleotide variant | not provided [RCV001455811] | Chr9:114168425 [GRCh38] Chr9:116930705 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3878C>T (p.Thr1293Met) | single nucleotide variant | Steel syndrome [RCV001559265]|not provided [RCV001511044] | Chr9:114282563 [GRCh38] Chr9:117044843 [GRCh37] Chr9:9q32 |
benign|likely benign |
NM_032888.4(COL27A1):c.3930T>C (p.Tyr1310=) | single nucleotide variant | not provided [RCV001478375] | Chr9:114283759 [GRCh38] Chr9:117046039 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.894C>A (p.Thr298=) | single nucleotide variant | not provided [RCV001485024] | Chr9:114168449 [GRCh38] Chr9:116930729 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3771+9C>A | single nucleotide variant | not provided [RCV001438321] | Chr9:114282339 [GRCh38] Chr9:117044619 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.636T>C (p.Ala212=) | single nucleotide variant | not provided [RCV001452187] | Chr9:114168191 [GRCh38] Chr9:116930471 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2269-4C>T | single nucleotide variant | not provided [RCV001440570] | Chr9:114209671 [GRCh38] Chr9:116971951 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2875T>C (p.Leu959=) | single nucleotide variant | not provided [RCV001443395] | Chr9:114242226 [GRCh38] Chr9:117004506 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3885T>C (p.Ala1295=) | single nucleotide variant | not provided [RCV001436586] | Chr9:114283714 [GRCh38] Chr9:117045994 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3453G>T (p.Pro1151=) | single nucleotide variant | not provided [RCV001423645] | Chr9:114267509 [GRCh38] Chr9:117029789 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3630G>C (p.Gly1210=) | single nucleotide variant | not provided [RCV001436866] | Chr9:114275681 [GRCh38] Chr9:117037961 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2328G>C (p.Leu776=) | single nucleotide variant | not provided [RCV001434173] | Chr9:114210987 [GRCh38] Chr9:116973267 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1518G>A (p.Thr506=) | single nucleotide variant | not provided [RCV001434205] | Chr9:114169073 [GRCh38] Chr9:116931353 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1459T>C (p.Leu487=) | single nucleotide variant | not provided [RCV001397799] | Chr9:114169014 [GRCh38] Chr9:116931294 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.417C>T (p.Leu139=) | single nucleotide variant | not provided [RCV001443609] | Chr9:114167972 [GRCh38] Chr9:116930252 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3492C>T (p.Ala1164=) | single nucleotide variant | not provided [RCV001459195] | Chr9:114267548 [GRCh38] Chr9:117029828 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3348G>A (p.Pro1116=) | single nucleotide variant | not provided [RCV001476565] | Chr9:114265430 [GRCh38] Chr9:117027710 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.891C>T (p.Pro297=) | single nucleotide variant | not provided [RCV001434727] | Chr9:114168446 [GRCh38] Chr9:116930726 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3210G>C (p.Pro1070=) | single nucleotide variant | not provided [RCV001425799] | Chr9:114264369 [GRCh38] Chr9:117026649 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.597T>C (p.Phe199=) | single nucleotide variant | not provided [RCV001418062] | Chr9:114168152 [GRCh38] Chr9:116930432 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2832C>T (p.Pro944=) | single nucleotide variant | not provided [RCV001503831] | Chr9:114240484 [GRCh38] Chr9:117002764 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4068C>T (p.Asp1356=) | single nucleotide variant | not provided [RCV001438664] | Chr9:114288725 [GRCh38] Chr9:117051005 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1311G>A (p.Pro437=) | single nucleotide variant | not provided [RCV001443714] | Chr9:114168866 [GRCh38] Chr9:116931146 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3327G>T (p.Ser1109=) | single nucleotide variant | not provided [RCV001476688] | Chr9:114265098 [GRCh38] Chr9:117027378 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.265G>A (p.Val89Ile) | single nucleotide variant | Steel syndrome [RCV001543746]|not provided [RCV001515162] | Chr9:114167820 [GRCh38] Chr9:116930100 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.359A>G (p.Gln120Arg) | single nucleotide variant | Steel syndrome [RCV001543747]|not provided [RCV001515163] | Chr9:114167914 [GRCh38] Chr9:116930194 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1610T>C (p.Ile537Thr) | single nucleotide variant | Steel syndrome [RCV001543749]|not provided [RCV001515164] | Chr9:114169165 [GRCh38] Chr9:116931445 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1902C>T (p.Gly634=) | single nucleotide variant | Steel syndrome [RCV001543773]|not provided [RCV001515165] | Chr9:114169457 [GRCh38] Chr9:116931737 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.57C>G (p.Arg19=) | single nucleotide variant | not provided [RCV001505492] | Chr9:114156007 [GRCh38] Chr9:116918287 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2367+2T>C | single nucleotide variant | not provided [RCV001377240] | Chr9:114211028 [GRCh38] Chr9:116973308 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.5244G>A (p.Gln1748=) | single nucleotide variant | not provided [RCV001402163] | Chr9:114309286 [GRCh38] Chr9:117071566 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5202C>A (p.Pro1734=) | single nucleotide variant | not provided [RCV001432901] | Chr9:114307763 [GRCh38] Chr9:117070043 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-5C>T | single nucleotide variant | not provided [RCV001432903] | Chr9:114250610 [GRCh38] Chr9:117012890 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4153-4G>A | single nucleotide variant | not provided [RCV001459387] | Chr9:114289238 [GRCh38] Chr9:117051518 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.90C>T (p.Val30=) | single nucleotide variant | not provided [RCV001461988] | Chr9:114162742 [GRCh38] Chr9:116925022 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1375C>T (p.Arg459Trp) | single nucleotide variant | not provided [RCV001463511] | Chr9:114168930 [GRCh38] Chr9:116931210 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2238G>A (p.Pro746=) | single nucleotide variant | not provided [RCV001463580] | Chr9:114206266 [GRCh38] Chr9:116968546 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4998A>G (p.Leu1666=) | single nucleotide variant | not provided [RCV001503923] | Chr9:114306579 [GRCh38] Chr9:117068859 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1341C>T (p.Thr447=) | single nucleotide variant | not provided [RCV001393835] | Chr9:114168896 [GRCh38] Chr9:116931176 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5103G>A (p.Val1701=) | single nucleotide variant | not provided [RCV001494154] | Chr9:114306684 [GRCh38] Chr9:117068964 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.882C>T (p.Pro294=) | single nucleotide variant | not provided [RCV001424351] | Chr9:114168437 [GRCh38] Chr9:116930717 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2631G>C (p.Gly877=) | single nucleotide variant | not provided [RCV001424467] | Chr9:114236992 [GRCh38] Chr9:116999272 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.549G>C (p.Leu183=) | single nucleotide variant | not provided [RCV001441466] | Chr9:114168104 [GRCh38] Chr9:116930384 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2457C>T (p.Pro819=) | single nucleotide variant | not provided [RCV001405081] | Chr9:114222258 [GRCh38] Chr9:116984538 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4005C>T (p.Asp1335=) | single nucleotide variant | not provided [RCV001450340] | Chr9:114288472 [GRCh38] Chr9:117050752 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2148G>T (p.Pro716=) | single nucleotide variant | Steel syndrome [RCV001543781]|not provided [RCV001512060] | Chr9:114205125 [GRCh38] Chr9:116967405 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2745C>T (p.Ile915=) | single nucleotide variant | Steel syndrome [RCV001543784]|not provided [RCV001512061] | Chr9:114240237 [GRCh38] Chr9:117002517 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3570T>C (p.Leu1190=) | single nucleotide variant | Steel syndrome [RCV001543787]|not provided [RCV001512062] | Chr9:114270742 [GRCh38] Chr9:117033022 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4061G>A (p.Arg1354Gln) | single nucleotide variant | Steel syndrome [RCV001543916]|not provided [RCV001512064] | Chr9:114288718 [GRCh38] Chr9:117050998 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1704G>A (p.Leu568=) | single nucleotide variant | not provided [RCV001426635] | Chr9:114169259 [GRCh38] Chr9:116931539 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3982G>A (p.Glu1328Lys) | single nucleotide variant | not provided [RCV001504211] | Chr9:114284772 [GRCh38] Chr9:117047052 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5580C>T (p.Leu1860=) | single nucleotide variant | not provided [RCV001468230] | Chr9:114310692 [GRCh38] Chr9:117072972 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2541G>A (p.Gly847=) | single nucleotide variant | not provided [RCV001399022] | Chr9:114231842 [GRCh38] Chr9:116994122 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4701+10C>T | single nucleotide variant | not provided [RCV001399051] | Chr9:114300697 [GRCh38] Chr9:117062977 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3609+1G>T | single nucleotide variant | not provided [RCV001377386] | Chr9:114270782 [GRCh38] Chr9:117033062 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4293G>A (p.Val1431=) | single nucleotide variant | not provided [RCV001428091] | Chr9:114290256 [GRCh38] Chr9:117052536 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4665A>G (p.Lys1555=) | single nucleotide variant | not provided [RCV001452573] | Chr9:114300651 [GRCh38] Chr9:117062931 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3084G>A (p.Ser1028=) | single nucleotide variant | not provided [RCV001416794] | Chr9:114252643 [GRCh38] Chr9:117014923 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3693C>A (p.Gly1231=) | single nucleotide variant | not provided [RCV001399103] | Chr9:114275744 [GRCh38] Chr9:117038024 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5415G>A (p.Glu1805=) | single nucleotide variant | not provided [RCV001484084] | Chr9:114309457 [GRCh38] Chr9:117071737 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.93G>T (p.Ser31=) | single nucleotide variant | not provided [RCV001437852] | Chr9:114162745 [GRCh38] Chr9:116925025 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4152+7_4152+10dup | duplication | not provided [RCV001401379] | Chr9:114288973..114288974 [GRCh38] Chr9:117051253..117051254 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5260C>T (p.Leu1754=) | single nucleotide variant | not provided [RCV001472272] | Chr9:114309302 [GRCh38] Chr9:117071582 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1829C>T (p.Ser610Leu) | single nucleotide variant | not provided [RCV001489677] | Chr9:114169384 [GRCh38] Chr9:116931664 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.20G>T (p.Arg7Leu) | single nucleotide variant | not provided [RCV001472459] | Chr9:114155970 [GRCh38] Chr9:116918250 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.235C>T (p.Arg79Trp) | single nucleotide variant | not provided [RCV001401169] | Chr9:114167790 [GRCh38] Chr9:116930070 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4368+7G>A | single nucleotide variant | not provided [RCV001501461] | Chr9:114290338 [GRCh38] Chr9:117052618 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1962+8A>T | single nucleotide variant | not provided [RCV001399175] | Chr9:114178352 [GRCh38] Chr9:116940632 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2157C>T (p.His719=) | single nucleotide variant | not provided [RCV001424884] | Chr9:114205134 [GRCh38] Chr9:116967414 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1635C>G (p.Ala545=) | single nucleotide variant | not provided [RCV001466902] | Chr9:114169190 [GRCh38] Chr9:116931470 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1332T>A (p.Pro444=) | single nucleotide variant | not provided [RCV001466945] | Chr9:114168887 [GRCh38] Chr9:116931167 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1896C>T (p.Asp632=) | single nucleotide variant | not provided [RCV001425003] | Chr9:114169451 [GRCh38] Chr9:116931731 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2320C>T (p.Arg774Ter) | single nucleotide variant | Steel syndrome [RCV002244252]|not provided [RCV003774694] | Chr9:114209726 [GRCh38] Chr9:116972006 [GRCh37] Chr9:9q32 |
pathogenic|likely pathogenic |
NM_032888.4(COL27A1):c.311T>C (p.Leu104Pro) | single nucleotide variant | not provided [RCV003108528] | Chr9:114167866 [GRCh38] Chr9:116930146 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4936G>A (p.Glu1646Lys) | single nucleotide variant | not provided [RCV003109189] | Chr9:114304671 [GRCh38] Chr9:117066951 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2368-2A>G | single nucleotide variant | not provided [RCV001772885] | Chr9:114219789 [GRCh38] Chr9:116982069 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1727G>T (p.Ser576Ile) | single nucleotide variant | Inborn genetic diseases [RCV002540723]|not provided [RCV002074048] | Chr9:114169282 [GRCh38] Chr9:116931562 [GRCh37] Chr9:9q32 |
likely benign|conflicting interpretations of pathogenicity|uncertain significance |
NM_032888.4(COL27A1):c.296C>T (p.Ala99Val) | single nucleotide variant | not provided [RCV001752675] | Chr9:114167851 [GRCh38] Chr9:116930131 [GRCh37] Chr9:9q32 |
conflicting interpretations of pathogenicity|uncertain significance |
NM_032888.4(COL27A1):c.2795C>A (p.Ala932Asp) | single nucleotide variant | not provided [RCV001752674] | Chr9:114240447 [GRCh38] Chr9:117002727 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3294+1G>C | single nucleotide variant | Steel syndrome [RCV001780545] | Chr9:114264969 [GRCh38] Chr9:117027249 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4060C>T (p.Arg1354Ter) | single nucleotide variant | Steel syndrome [RCV001815630]|not provided [RCV001869636] | Chr9:114288717 [GRCh38] Chr9:117050997 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.60G>T (p.Gly20=) | single nucleotide variant | not provided [RCV001929548] | Chr9:114156010 [GRCh38] Chr9:116918290 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.818C>G (p.Thr273Ser) | single nucleotide variant | not provided [RCV002045588] | Chr9:114168373 [GRCh38] Chr9:116930653 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4526C>G (p.Thr1509Arg) | single nucleotide variant | not provided [RCV001970538] | Chr9:114292152 [GRCh38] Chr9:117054432 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3771+2_3771+3delinsAG | indel | not provided [RCV002045600] | Chr9:114282332..114282333 [GRCh38] Chr9:117044612..117044613 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.1235G>T (p.Arg412Leu) | single nucleotide variant | not provided [RCV002009203] | Chr9:114168790 [GRCh38] Chr9:116931070 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3493G>A (p.Gly1165Arg) | single nucleotide variant | not provided [RCV002025439] | Chr9:114267549 [GRCh38] Chr9:117029829 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2065del (p.Ala689fs) | deletion | not provided [RCV001949624] | Chr9:114194449 [GRCh38] Chr9:116956729 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.5059G>A (p.Ala1687Thr) | single nucleotide variant | not provided [RCV002025275] | Chr9:114306640 [GRCh38] Chr9:117068920 [GRCh37] Chr9:9q32 |
uncertain significance |
GRCh37/hg19 9q32-33.1(chr9:116506015-119942279) | copy number loss | not specified [RCV002052832] | Chr9:116506015..119942279 [GRCh37] Chr9:9q32-33.1 |
uncertain significance |
NM_032888.4(COL27A1):c.530G>T (p.Arg177Leu) | single nucleotide variant | not provided [RCV001908194] | Chr9:114168085 [GRCh38] Chr9:116930365 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2576_2577insT (p.Val860fs) | insertion | not provided [RCV001874731] | Chr9:114235609..114235610 [GRCh38] Chr9:116997889..116997890 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3616del (p.Arg1206fs) | deletion | not provided [RCV001929821] | Chr9:114275667 [GRCh38] Chr9:117037947 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1962+1G>A | single nucleotide variant | not provided [RCV002025166] | Chr9:114178345 [GRCh38] Chr9:116940625 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3758G>T (p.Arg1253Leu) | single nucleotide variant | not provided [RCV001928682] | Chr9:114282317 [GRCh38] Chr9:117044597 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4588G>A (p.Asp1530Asn) | single nucleotide variant | not provided [RCV001949905] | Chr9:114300073 [GRCh38] Chr9:117062353 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2237C>T (p.Pro746Leu) | single nucleotide variant | not provided [RCV001909216] | Chr9:114206265 [GRCh38] Chr9:116968545 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2980-17G>A | single nucleotide variant | not provided [RCV001966020] | Chr9:114250598 [GRCh38] Chr9:117012878 [GRCh37] Chr9:9q32 |
uncertain significance |
GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389) | copy number gain | not specified [RCV002053823] | Chr9:353349..141020389 [GRCh37] Chr9:9p24.3-q34.3 |
pathogenic |
NM_032888.4(COL27A1):c.205C>A (p.Pro69Thr) | single nucleotide variant | not provided [RCV002041929] | Chr9:114167760 [GRCh38] Chr9:116930040 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4290C>T (p.Gly1430=) | single nucleotide variant | not provided [RCV001967817] | Chr9:114290253 [GRCh38] Chr9:117052533 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.1208C>T (p.Thr403Ile) | single nucleotide variant | not provided [RCV002020848] | Chr9:114168763 [GRCh38] Chr9:116931043 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.62+1G>C | single nucleotide variant | not provided [RCV002040724] | Chr9:114156013 [GRCh38] Chr9:116918293 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2995A>G (p.Ile999Val) | single nucleotide variant | not provided [RCV001983881] | Chr9:114250630 [GRCh38] Chr9:117012910 [GRCh37] Chr9:9q32 |
uncertain significance |
GRCh37/hg19 9q32-34.11(chr9:116422275-131713233) | copy number gain | not specified [RCV002052831] | Chr9:116422275..131713233 [GRCh37] Chr9:9q32-34.11 |
pathogenic |
NM_032888.4(COL27A1):c.4025del (p.Pro1342fs) | deletion | not provided [RCV001970090] | Chr9:114288488 [GRCh38] Chr9:117050768 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1517C>G (p.Thr506Arg) | single nucleotide variant | not provided [RCV001969404] | Chr9:114169072 [GRCh38] Chr9:116931352 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3771+2T>C | single nucleotide variant | not provided [RCV001966327] | Chr9:114282332 [GRCh38] Chr9:117044612 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.391C>T (p.Leu131Phe) | single nucleotide variant | not provided [RCV001928221] | Chr9:114167946 [GRCh38] Chr9:116930226 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4152+8G>A | single nucleotide variant | not provided [RCV001908373] | Chr9:114288975 [GRCh38] Chr9:117051255 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2535C>A (p.Ser845Arg) | single nucleotide variant | Inborn genetic diseases [RCV003339899]|not provided [RCV002021182] | Chr9:114231836 [GRCh38] Chr9:116994116 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.676C>A (p.His226Asn) | single nucleotide variant | not provided [RCV001945944] | Chr9:114168231 [GRCh38] Chr9:116930511 [GRCh37] Chr9:9q32 |
uncertain significance |
GRCh37/hg19 9q31.1-33.3(chr9:104604851-126253089) | copy number loss | not specified [RCV002052825] | Chr9:104604851..126253089 [GRCh37] Chr9:9q31.1-33.3 |
pathogenic |
NM_032888.4(COL27A1):c.1602G>C (p.Lys534Asn) | single nucleotide variant | not provided [RCV001970018] | Chr9:114169157 [GRCh38] Chr9:116931437 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2542del (p.Glu848fs) | deletion | not provided [RCV001949001] | Chr9:114231839 [GRCh38] Chr9:116994119 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.62+1G>T | single nucleotide variant | Steel syndrome [RCV001823467]|not provided [RCV002545191] | Chr9:114156013 [GRCh38] Chr9:116918293 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2367G>A (p.Pro789=) | single nucleotide variant | Steel syndrome [RCV003317536]|not provided [RCV002041698] | Chr9:114211026 [GRCh38] Chr9:116973306 [GRCh37] Chr9:9q32 |
likely pathogenic |
GRCh37/hg19 9q31.2-32(chr9:109265628-117650999) | copy number loss | not specified [RCV002052828] | Chr9:109265628..117650999 [GRCh37] Chr9:9q31.2-32 |
likely pathogenic |
NM_032888.4(COL27A1):c.62+5G>C | single nucleotide variant | not provided [RCV001911075] | Chr9:114156017 [GRCh38] Chr9:116918297 [GRCh37] Chr9:9q32 |
uncertain significance |
GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410) | copy number gain | not specified [RCV002053853] | Chr9:71349994..122603410 [GRCh37] Chr9:9q21.11-33.2 |
likely pathogenic |
NM_032888.4(COL27A1):c.1567G>C (p.Val523Leu) | single nucleotide variant | not provided [RCV001947322] | Chr9:114169122 [GRCh38] Chr9:116931402 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5539G>T (p.Gly1847Trp) | single nucleotide variant | not provided [RCV001927337] | Chr9:114310651 [GRCh38] Chr9:117072931 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3893G>T (p.Arg1298Leu) | single nucleotide variant | not provided [RCV001948711] | Chr9:114283722 [GRCh38] Chr9:117046002 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.269T>C (p.Ile90Thr) | single nucleotide variant | not provided [RCV001872578] | Chr9:114167824 [GRCh38] Chr9:116930104 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4938+2_4938+15del | deletion | not provided [RCV001969450] | Chr9:114304675..114304688 [GRCh38] Chr9:117066955..117066968 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2980-2A>G | single nucleotide variant | not provided [RCV002005501] | Chr9:114250613 [GRCh38] Chr9:117012893 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4559G>A (p.Gly1520Glu) | single nucleotide variant | not provided [RCV002002229] | Chr9:114292185 [GRCh38] Chr9:117054465 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3249+8C>T | single nucleotide variant | not provided [RCV002184967] | Chr9:114264416 [GRCh38] Chr9:117026696 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1612G>A (p.Gly538Arg) | single nucleotide variant | not provided [RCV001997437] | Chr9:114169167 [GRCh38] Chr9:116931447 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1444C>G (p.Pro482Ala) | single nucleotide variant | not provided [RCV001867229] | Chr9:114168999 [GRCh38] Chr9:116931279 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5033C>T (p.Thr1678Met) | single nucleotide variant | not provided [RCV002001208] | Chr9:114306614 [GRCh38] Chr9:117068894 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2823G>C (p.Gln941His) | single nucleotide variant | not provided [RCV001880525] | Chr9:114240475 [GRCh38] Chr9:117002755 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2323-17C>T | single nucleotide variant | not provided [RCV001939390] | Chr9:114210965 [GRCh38] Chr9:116973245 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2961G>C (p.Pro987=) | single nucleotide variant | not provided [RCV001962892] | Chr9:114245892 [GRCh38] Chr9:117008172 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3229C>G (p.Gln1077Glu) | single nucleotide variant | not provided [RCV001944102] | Chr9:114264388 [GRCh38] Chr9:117026668 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1914_1922dup (p.641LPG[3]) | duplication | not provided [RCV001935539] | Chr9:114178295..114178296 [GRCh38] Chr9:116940575..116940576 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2880+1G>A | single nucleotide variant | not provided [RCV002010925] | Chr9:114242232 [GRCh38] Chr9:117004512 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4938+1G>A | single nucleotide variant | not provided [RCV002038674] | Chr9:114304674 [GRCh38] Chr9:117066954 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.1669C>T (p.Leu557Phe) | single nucleotide variant | Inborn genetic diseases [RCV003375430]|not provided [RCV001918479] | Chr9:114169224 [GRCh38] Chr9:116931504 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1373del (p.Ala458fs) | deletion | not provided [RCV002035260] | Chr9:114168928 [GRCh38] Chr9:116931208 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3554G>A (p.Arg1185Gln) | single nucleotide variant | Inborn genetic diseases [RCV002561557]|not provided [RCV001962689] | Chr9:114269293 [GRCh38] Chr9:117031573 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4760del (p.Pro1587fs) | deletion | not provided [RCV002037941] | Chr9:114301287 [GRCh38] Chr9:117063567 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3250-2A>G | single nucleotide variant | not provided [RCV002038819] | Chr9:114264922 [GRCh38] Chr9:117027202 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2778G>A (p.Met926Ile) | single nucleotide variant | not provided [RCV002047982] | Chr9:114240270 [GRCh38] Chr9:117002550 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4938+1G>C | single nucleotide variant | not provided [RCV001992179] | Chr9:114304674 [GRCh38] Chr9:117066954 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3914C>T (p.Pro1305Leu) | single nucleotide variant | not provided [RCV001919036] | Chr9:114283743 [GRCh38] Chr9:117046023 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.11G>C (p.Gly4Ala) | single nucleotide variant | not provided [RCV001989771] | Chr9:114155961 [GRCh38] Chr9:116918241 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1988C>T (p.Pro663Leu) | single nucleotide variant | not provided [RCV002010497] | Chr9:114183047 [GRCh38] Chr9:116945327 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4121T>C (p.Leu1374Pro) | single nucleotide variant | not provided [RCV002030776] | Chr9:114288936 [GRCh38] Chr9:117051216 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1023T>C (p.Val341=) | single nucleotide variant | not provided [RCV001920671] | Chr9:114168578 [GRCh38] Chr9:116930858 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3577G>T (p.Asp1193Tyr) | single nucleotide variant | not provided [RCV002050945] | Chr9:114270749 [GRCh38] Chr9:117033029 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4351G>C (p.Gly1451Arg) | single nucleotide variant | not provided [RCV002048484]|not specified [RCV003331273] | Chr9:114290314 [GRCh38] Chr9:117052594 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3083dup (p.Met1029fs) | duplication | not provided [RCV001864885] | Chr9:114252641..114252642 [GRCh38] Chr9:117014921..117014922 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1258C>T (p.Arg420Cys) | single nucleotide variant | not provided [RCV001956628] | Chr9:114168813 [GRCh38] Chr9:116931093 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.490C>T (p.Arg164Ter) | single nucleotide variant | not provided [RCV001953531] | Chr9:114168045 [GRCh38] Chr9:116930325 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2026G>A (p.Gly676Arg) | single nucleotide variant | not provided [RCV001991618] | Chr9:114194413 [GRCh38] Chr9:116956693 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4238C>A (p.Ala1413Asp) | single nucleotide variant | not provided [RCV002047431] | Chr9:114290089 [GRCh38] Chr9:117052369 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3806T>C (p.Met1269Thr) | single nucleotide variant | not provided [RCV001876894] | Chr9:114282491 [GRCh38] Chr9:117044771 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3249+1G>T | single nucleotide variant | not provided [RCV002050013] | Chr9:114264409 [GRCh38] Chr9:117026689 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.521G>C (p.Cys174Ser) | single nucleotide variant | not provided [RCV001878360] | Chr9:114168076 [GRCh38] Chr9:116930356 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3680_3692del (p.Asp1227fs) | deletion | not provided [RCV001994752] | Chr9:114275729..114275741 [GRCh38] Chr9:117038009..117038021 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4068C>A (p.Asp1356Glu) | single nucleotide variant | not provided [RCV001922820] | Chr9:114288725 [GRCh38] Chr9:117051005 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1966C>T (p.Pro656Ser) | single nucleotide variant | not provided [RCV001974907] | Chr9:114183025 [GRCh38] Chr9:116945305 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4958G>T (p.Arg1653Leu) | single nucleotide variant | not provided [RCV001902082] | Chr9:114306539 [GRCh38] Chr9:117068819 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.484G>A (p.Glu162Lys) | single nucleotide variant | not provided [RCV002014770] | Chr9:114168039 [GRCh38] Chr9:116930319 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4810-22TCT[2] | microsatellite | not provided [RCV002017885] | Chr9:114301660..114301662 [GRCh38] Chr9:117063940..117063942 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3141+4A>C | single nucleotide variant | not provided [RCV001995112] | Chr9:114252936 [GRCh38] Chr9:117015216 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1521_1523del (p.Met507_Val508delinsIle) | deletion | not provided [RCV001880917] | Chr9:114169075..114169077 [GRCh38] Chr9:116931355..116931357 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2114C>T (p.Pro705Leu) | single nucleotide variant | not provided [RCV001979729] | Chr9:114196002 [GRCh38] Chr9:116958282 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2374C>A (p.Pro792Thr) | single nucleotide variant | not provided [RCV001979798] | Chr9:114219797 [GRCh38] Chr9:116982077 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.923C>G (p.Pro308Arg) | single nucleotide variant | not provided [RCV002018641] | Chr9:114168478 [GRCh38] Chr9:116930758 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3700G>A (p.Gly1234Ser) | single nucleotide variant | not provided [RCV001886098] | Chr9:114275751 [GRCh38] Chr9:117038031 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5373G>A (p.Trp1791Ter) | single nucleotide variant | not provided [RCV001939536] | Chr9:114309415 [GRCh38] Chr9:117071695 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.924_927dup (p.Gln310fs) | duplication | not provided [RCV001925532] | Chr9:114168477..114168478 [GRCh38] Chr9:116930757..116930758 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2139T>A (p.Tyr713Ter) | single nucleotide variant | not provided [RCV001926135] | Chr9:114205116 [GRCh38] Chr9:116967396 [GRCh37] Chr9:9q32 |
pathogenic |
NC_000009.11:g.(?_117044259)_(117046337_?)del | deletion | not provided [RCV002026538] | Chr9:117044259..117046337 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.334G>A (p.Ala112Thr) | single nucleotide variant | not provided [RCV001877189] | Chr9:114167889 [GRCh38] Chr9:116930169 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1450T>C (p.Phe484Leu) | single nucleotide variant | not provided [RCV001922097] | Chr9:114169005 [GRCh38] Chr9:116931285 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5177A>G (p.His1726Arg) | single nucleotide variant | Inborn genetic diseases [RCV002657714]|not provided [RCV002028681] | Chr9:114307738 [GRCh38] Chr9:117070018 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4643C>T (p.Pro1548Leu) | single nucleotide variant | not provided [RCV001939123] | Chr9:114300629 [GRCh38] Chr9:117062909 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4560G>A (p.Gly1520=) | single nucleotide variant | not provided [RCV001960743] | Chr9:114292186 [GRCh38] Chr9:117054466 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2399C>T (p.Pro800Leu) | single nucleotide variant | not provided [RCV002027025] | Chr9:114219822 [GRCh38] Chr9:116982102 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.323G>A (p.Arg108Gln) | single nucleotide variant | not provided [RCV001900731] | Chr9:114167878 [GRCh38] Chr9:116930158 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2226G>T (p.Gly742=) | single nucleotide variant | not provided [RCV001994514] | Chr9:114206254 [GRCh38] Chr9:116968534 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4938+1G>T | single nucleotide variant | not provided [RCV002015039] | Chr9:114304674 [GRCh38] Chr9:117066954 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3821A>T (p.Asp1274Val) | single nucleotide variant | not provided [RCV001936330] | Chr9:114282506 [GRCh38] Chr9:117044786 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1345_1346delinsAA (p.Ser449Asn) | indel | not provided [RCV001875620] | Chr9:114168900..114168901 [GRCh38] Chr9:116931180..116931181 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4120C>G (p.Leu1374Val) | single nucleotide variant | Inborn genetic diseases [RCV002554208]|not provided [RCV001898657] | Chr9:114288935 [GRCh38] Chr9:117051215 [GRCh37] Chr9:9q32 |
likely benign|conflicting interpretations of pathogenicity|uncertain significance |
NM_032888.4(COL27A1):c.3615C>T (p.Asp1205=) | single nucleotide variant | not provided [RCV002091968] | Chr9:114275666 [GRCh38] Chr9:117037946 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3880-7C>T | single nucleotide variant | not provided [RCV002166049] | Chr9:114283702 [GRCh38] Chr9:117045982 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4995C>T (p.Thr1665=) | single nucleotide variant | not provided [RCV002075344] | Chr9:114306576 [GRCh38] Chr9:117068856 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2751C>T (p.Pro917=) | single nucleotide variant | not provided [RCV002090045] | Chr9:114240243 [GRCh38] Chr9:117002523 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4206+10_4206+11inv | inversion | not provided [RCV002075431] | Chr9:114289305..114289306 [GRCh38] Chr9:117051585..117051586 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4477-7C>A | single nucleotide variant | not provided [RCV002076398] | Chr9:114292096 [GRCh38] Chr9:117054376 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2445C>G (p.Pro815=) | single nucleotide variant | not provided [RCV002185532] | Chr9:114222246 [GRCh38] Chr9:116984526 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5437-9T>C | single nucleotide variant | not provided [RCV002190434] | Chr9:114310540 [GRCh38] Chr9:117072820 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2071-7C>T | single nucleotide variant | not provided [RCV002071508] | Chr9:114195952 [GRCh38] Chr9:116958232 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.795C>T (p.Ala265=) | single nucleotide variant | not provided [RCV002188882] | Chr9:114168350 [GRCh38] Chr9:116930630 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1950A>G (p.Ala650=) | single nucleotide variant | not provided [RCV002188965] | Chr9:114178332 [GRCh38] Chr9:116940612 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2467-7C>T | single nucleotide variant | not provided [RCV002071790] | Chr9:114231072 [GRCh38] Chr9:116993352 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4368+16C>T | single nucleotide variant | not provided [RCV002126752] | Chr9:114290347 [GRCh38] Chr9:117052627 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4791+7G>C | single nucleotide variant | not provided [RCV002145199] | Chr9:114301326 [GRCh38] Chr9:117063606 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3771+10C>T | single nucleotide variant | not provided [RCV002207702] | Chr9:114282340 [GRCh38] Chr9:117044620 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4545C>A (p.Leu1515=) | single nucleotide variant | not provided [RCV002108793] | Chr9:114292171 [GRCh38] Chr9:117054451 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2322+9G>C | single nucleotide variant | not provided [RCV002108849] | Chr9:114209737 [GRCh38] Chr9:116972017 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4281G>A (p.Gly1427=) | single nucleotide variant | not provided [RCV002145505] | Chr9:114290244 [GRCh38] Chr9:117052524 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2323-8C>A | single nucleotide variant | not provided [RCV002090685] | Chr9:114210974 [GRCh38] Chr9:116973254 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2382C>T (p.Val794=) | single nucleotide variant | not provided [RCV002207983] | Chr9:114219805 [GRCh38] Chr9:116982085 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2589G>A (p.Val863=) | single nucleotide variant | not provided [RCV002127693] | Chr9:114235622 [GRCh38] Chr9:116997902 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2625C>T (p.Ser875=) | single nucleotide variant | not provided [RCV002072374] | Chr9:114236986 [GRCh38] Chr9:116999266 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4701+7T>A | single nucleotide variant | not provided [RCV002205072] | Chr9:114300694 [GRCh38] Chr9:117062974 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2811A>G (p.Gly937=) | single nucleotide variant | not provided [RCV002205161] | Chr9:114240463 [GRCh38] Chr9:117002743 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.42G>T (p.Ala14=) | single nucleotide variant | not provided [RCV002185298] | Chr9:114155992 [GRCh38] Chr9:116918272 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5218-24_5218-15del | deletion | not provided [RCV002072643] | Chr9:114309232..114309241 [GRCh38] Chr9:117071512..117071521 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2673+10T>C | single nucleotide variant | not provided [RCV002209843] | Chr9:114237044 [GRCh38] Chr9:116999324 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4099-18TC[4] | microsatellite | not provided [RCV002109273] | Chr9:114288895..114288896 [GRCh38] Chr9:117051175..117051176 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2928C>G (p.Gly976=) | single nucleotide variant | not provided [RCV002130735] | Chr9:114243554 [GRCh38] Chr9:117005834 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2881-17C>A | single nucleotide variant | not provided [RCV002110030] | Chr9:114243490 [GRCh38] Chr9:117005770 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4044+19C>G | single nucleotide variant | not provided [RCV002129707] | Chr9:114288530 [GRCh38] Chr9:117050810 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4873-8_4873-5dup | duplication | not provided [RCV002189883] | Chr9:114304598..114304599 [GRCh38] Chr9:117066878..117066879 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3972A>G (p.Gly1324=) | single nucleotide variant | not provided [RCV002192976] | Chr9:114284762 [GRCh38] Chr9:117047042 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.835C>T (p.Leu279=) | single nucleotide variant | not provided [RCV002165010] | Chr9:114168390 [GRCh38] Chr9:116930670 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.930G>A (p.Gln310=) | single nucleotide variant | not provided [RCV002089888] | Chr9:114168485 [GRCh38] Chr9:116930765 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3772-10C>G | single nucleotide variant | not provided [RCV002169477] | Chr9:114282447 [GRCh38] Chr9:117044727 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3448-13C>T | single nucleotide variant | not provided [RCV002105011] | Chr9:114267491 [GRCh38] Chr9:117029771 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4846-6T>C | single nucleotide variant | not provided [RCV002110228] | Chr9:114302076 [GRCh38] Chr9:117064356 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2368-10T>C | single nucleotide variant | not provided [RCV002148895] | Chr9:114219781 [GRCh38] Chr9:116982061 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1815G>T (p.Thr605=) | single nucleotide variant | not provided [RCV002090267] | Chr9:114169370 [GRCh38] Chr9:116931650 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5218-15G>A | single nucleotide variant | not provided [RCV002148886] | Chr9:114309245 [GRCh38] Chr9:117071525 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4962G>A (p.Leu1654=) | single nucleotide variant | not provided [RCV002170222] | Chr9:114306543 [GRCh38] Chr9:117068823 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2071-13C>T | single nucleotide variant | not provided [RCV002186690] | Chr9:114195946 [GRCh38] Chr9:116958226 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.408C>A (p.Val136=) | single nucleotide variant | not provided [RCV002107645] | Chr9:114167963 [GRCh38] Chr9:116930243 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5061C>T (p.Ala1687=) | single nucleotide variant | not provided [RCV002208909] | Chr9:114306642 [GRCh38] Chr9:117068922 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2960C>T (p.Pro987Leu) | single nucleotide variant | not provided [RCV002145541] | Chr9:114245891 [GRCh38] Chr9:117008171 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4257C>G (p.Val1419=) | single nucleotide variant | not provided [RCV002209105] | Chr9:114290108 [GRCh38] Chr9:117052388 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.537G>A (p.Val179=) | single nucleotide variant | not provided [RCV002109050] | Chr9:114168092 [GRCh38] Chr9:116930372 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2538G>A (p.Val846=) | single nucleotide variant | not provided [RCV002186065] | Chr9:114231839 [GRCh38] Chr9:116994119 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2757C>A (p.Gly919=) | single nucleotide variant | not provided [RCV002207648] | Chr9:114240249 [GRCh38] Chr9:117002529 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3090T>C (p.Gly1030=) | single nucleotide variant | not provided [RCV002168461] | Chr9:114252881 [GRCh38] Chr9:117015161 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3225G>C (p.Gly1075=) | single nucleotide variant | not provided [RCV002129445] | Chr9:114264384 [GRCh38] Chr9:117026664 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3291G>A (p.Gln1097=) | single nucleotide variant | not provided [RCV002088213] | Chr9:114264965 [GRCh38] Chr9:117027245 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3460G>A (p.Ala1154Thr) | single nucleotide variant | not provided [RCV002207798] | Chr9:114267516 [GRCh38] Chr9:117029796 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4585-5T>C | single nucleotide variant | not provided [RCV002106914] | Chr9:114300065 [GRCh38] Chr9:117062345 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2835+15C>T | single nucleotide variant | not provided [RCV002210019] | Chr9:114240502 [GRCh38] Chr9:117002782 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3502-7C>T | single nucleotide variant | not provided [RCV002191050] | Chr9:114269234 [GRCh38] Chr9:117031514 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2169+12A>G | single nucleotide variant | not provided [RCV002124882] | Chr9:114205158 [GRCh38] Chr9:116967438 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1086C>T (p.Thr362=) | single nucleotide variant | not provided [RCV002086783] | Chr9:114168641 [GRCh38] Chr9:116930921 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.324G>A (p.Arg108=) | single nucleotide variant | not provided [RCV002206316] | Chr9:114167879 [GRCh38] Chr9:116930159 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.219C>T (p.Gly73=) | single nucleotide variant | not provided [RCV002074498] | Chr9:114167774 [GRCh38] Chr9:116930054 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4153-4G>T | single nucleotide variant | not provided [RCV002169161] | Chr9:114289238 [GRCh38] Chr9:117051518 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3339+9_3339+10delinsTT | indel | not provided [RCV002166423] | Chr9:114265119..114265120 [GRCh38] Chr9:117027399..117027400 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3568C>T (p.Leu1190Phe) | single nucleotide variant | Inborn genetic diseases [RCV003161439]|not provided [RCV002075044] | Chr9:114270740 [GRCh38] Chr9:117033020 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.5271C>G (p.Ser1757=) | single nucleotide variant | not provided [RCV002205430] | Chr9:114309313 [GRCh38] Chr9:117071593 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4846-89C>T | single nucleotide variant | not provided [RCV002223605] | Chr9:114301993 [GRCh38] Chr9:117064273 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.147C>T (p.Leu49=) | single nucleotide variant | not provided [RCV002075320] | Chr9:114167702 [GRCh38] Chr9:116929982 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3192T>C (p.Arg1064=) | single nucleotide variant | not provided [RCV002088708] | Chr9:114258591 [GRCh38] Chr9:117020871 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.134-9C>A | single nucleotide variant | not provided [RCV002210596] | Chr9:114167680 [GRCh38] Chr9:116929960 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1300A>C (p.Arg434=) | single nucleotide variant | not provided [RCV002130335] | Chr9:114168855 [GRCh38] Chr9:116931135 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2196A>G (p.Pro732=) | single nucleotide variant | not provided [RCV002209888] | Chr9:114205785 [GRCh38] Chr9:116968065 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1701C>T (p.Pro567=) | single nucleotide variant | not provided [RCV002169694] | Chr9:114169256 [GRCh38] Chr9:116931536 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.792C>T (p.Leu264=) | single nucleotide variant | not provided [RCV002166251] | Chr9:114168347 [GRCh38] Chr9:116930627 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2313T>C (p.Asp771=) | single nucleotide variant | not provided [RCV002190354] | Chr9:114209719 [GRCh38] Chr9:116971999 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4791+7G>A | single nucleotide variant | not provided [RCV002092120] | Chr9:114301326 [GRCh38] Chr9:117063606 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.295G>A (p.Ala99Thr) | single nucleotide variant | not provided [RCV002067711]|not specified [RCV003396618] | Chr9:114167850 [GRCh38] Chr9:116930130 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.2736A>C (p.Pro912=) | single nucleotide variant | not provided [RCV002097726] | Chr9:114240228 [GRCh38] Chr9:117002508 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2269-5C>T | single nucleotide variant | not provided [RCV002079436] | Chr9:114209670 [GRCh38] Chr9:116971950 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.21G>C (p.Arg7=) | single nucleotide variant | not provided [RCV002145760] | Chr9:114155971 [GRCh38] Chr9:116918251 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1869G>C (p.Leu623=) | single nucleotide variant | not provided [RCV002194992] | Chr9:114169424 [GRCh38] Chr9:116931704 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2934+10C>T | single nucleotide variant | not provided [RCV002174773] | Chr9:114243570 [GRCh38] Chr9:117005850 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5094G>A (p.Gln1698=) | single nucleotide variant | not provided [RCV002117228] | Chr9:114306675 [GRCh38] Chr9:117068955 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2170-8C>T | single nucleotide variant | not provided [RCV002171004] | Chr9:114205751 [GRCh38] Chr9:116968031 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.12A>G (p.Gly4=) | single nucleotide variant | not provided [RCV002084817] | Chr9:114155962 [GRCh38] Chr9:116918242 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3610-18T>G | single nucleotide variant | not provided [RCV002097300] | Chr9:114275643 [GRCh38] Chr9:117037923 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4755+7G>T | single nucleotide variant | not provided [RCV002074773] | Chr9:114301132 [GRCh38] Chr9:117063412 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3477C>A (p.Gly1159=) | single nucleotide variant | not provided [RCV002077057] | Chr9:114267533 [GRCh38] Chr9:117029813 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.471C>T (p.His157=) | single nucleotide variant | not provided [RCV002104637] | Chr9:114168026 [GRCh38] Chr9:116930306 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3348G>T (p.Pro1116=) | single nucleotide variant | not provided [RCV002130856] | Chr9:114265430 [GRCh38] Chr9:117027710 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3142-10C>A | single nucleotide variant | not provided [RCV002112984] | Chr9:114258531 [GRCh38] Chr9:117020811 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4689A>G (p.Pro1563=) | single nucleotide variant | not provided [RCV002149620] | Chr9:114300675 [GRCh38] Chr9:117062955 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.547C>T (p.Leu183=) | single nucleotide variant | not provided [RCV002134582] | Chr9:114168102 [GRCh38] Chr9:116930382 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.534G>A (p.Arg178=) | single nucleotide variant | not provided [RCV002127083] | Chr9:114168089 [GRCh38] Chr9:116930369 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3867C>T (p.Ser1289=) | single nucleotide variant | not provided [RCV002072891] | Chr9:114282552 [GRCh38] Chr9:117044832 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.576C>T (p.Asp192=) | single nucleotide variant | not provided [RCV002193945] | Chr9:114168131 [GRCh38] Chr9:116930411 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.828A>G (p.Thr276=) | single nucleotide variant | not provided [RCV002134742] | Chr9:114168383 [GRCh38] Chr9:116930663 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4639-7C>T | single nucleotide variant | not provided [RCV002094655] | Chr9:114300618 [GRCh38] Chr9:117062898 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3250-10C>T | single nucleotide variant | not provided [RCV002188463] | Chr9:114264914 [GRCh38] Chr9:117027194 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4042C>A (p.Arg1348=) | single nucleotide variant | not provided [RCV002190025] | Chr9:114288509 [GRCh38] Chr9:117050789 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4099-8G>C | single nucleotide variant | not provided [RCV002149898] | Chr9:114288906 [GRCh38] Chr9:117051186 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4701+17C>T | single nucleotide variant | not provided [RCV002116094] | Chr9:114300704 [GRCh38] Chr9:117062984 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2466+15G>T | single nucleotide variant | not provided [RCV002174432] | Chr9:114222282 [GRCh38] Chr9:116984562 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3987+7G>A | single nucleotide variant | not provided [RCV002170511] | Chr9:114284784 [GRCh38] Chr9:117047064 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1734_1743dup (p.Pro582fs) | duplication | not provided [RCV001945009] | Chr9:114169280..114169281 [GRCh38] Chr9:116931560..116931561 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1764G>A (p.Pro588=) | single nucleotide variant | not provided [RCV002127940] | Chr9:114169319 [GRCh38] Chr9:116931599 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2323-15G>C | single nucleotide variant | not provided [RCV002109714] | Chr9:114210967 [GRCh38] Chr9:116973247 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3879+10C>G | single nucleotide variant | not provided [RCV002148186] | Chr9:114282574 [GRCh38] Chr9:117044854 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.170C>T (p.Thr57Met) | single nucleotide variant | Inborn genetic diseases [RCV002550521]|not provided [RCV002077615] | Chr9:114167725 [GRCh38] Chr9:116930005 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.2418T>C (p.Asn806=) | single nucleotide variant | not provided [RCV002096973] | Chr9:114219841 [GRCh38] Chr9:116982121 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4311C>A (p.Leu1437=) | single nucleotide variant | not provided [RCV002113450] | Chr9:114290274 [GRCh38] Chr9:117052554 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2070+8del | deletion | not provided [RCV002205551] | Chr9:114194463 [GRCh38] Chr9:116956743 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2169+11C>T | single nucleotide variant | not provided [RCV002148290] | Chr9:114205157 [GRCh38] Chr9:116967437 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4476+20A>C | single nucleotide variant | not provided [RCV002095237] | Chr9:114290937 [GRCh38] Chr9:117053217 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2538G>T (p.Val846=) | single nucleotide variant | not provided [RCV002078755] | Chr9:114231839 [GRCh38] Chr9:116994119 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.750C>T (p.Phe250=) | single nucleotide variant | not provided [RCV002173348] | Chr9:114168305 [GRCh38] Chr9:116930585 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4026T>C (p.Pro1342=) | single nucleotide variant | not provided [RCV002097020] | Chr9:114288493 [GRCh38] Chr9:117050773 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4248G>T (p.Arg1416=) | single nucleotide variant | not provided [RCV002134990] | Chr9:114290099 [GRCh38] Chr9:117052379 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1821T>C (p.Ser607=) | single nucleotide variant | not provided [RCV002216020] | Chr9:114169376 [GRCh38] Chr9:116931656 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1374T>G (p.Ala458=) | single nucleotide variant | not provided [RCV002079298] | Chr9:114168929 [GRCh38] Chr9:116931209 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2654G>A (p.Arg885Gln) | single nucleotide variant | Inborn genetic diseases [RCV003015284]|not provided [RCV002117080] | Chr9:114237015 [GRCh38] Chr9:116999295 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.801A>G (p.Leu267=) | single nucleotide variant | not provided [RCV002108350] | Chr9:114168356 [GRCh38] Chr9:116930636 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2269-6T>C | single nucleotide variant | not provided [RCV002196460] | Chr9:114209669 [GRCh38] Chr9:116971949 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4278A>T (p.Pro1426=) | single nucleotide variant | not provided [RCV002133033] | Chr9:114290241 [GRCh38] Chr9:117052521 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4791+16G>A | single nucleotide variant | not provided [RCV002207064] | Chr9:114301335 [GRCh38] Chr9:117063615 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1566C>G (p.Ala522=) | single nucleotide variant | not provided [RCV002126802] | Chr9:114169121 [GRCh38] Chr9:116931401 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3957C>T (p.Pro1319=) | single nucleotide variant | not provided [RCV002169934] | Chr9:114284747 [GRCh38] Chr9:117047027 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3717+19T>A | single nucleotide variant | not provided [RCV002132333] | Chr9:114275787 [GRCh38] Chr9:117038067 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.133+12T>C | single nucleotide variant | not provided [RCV002094567] | Chr9:114162797 [GRCh38] Chr9:116925077 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2934+14G>C | single nucleotide variant | not provided [RCV002195459] | Chr9:114243574 [GRCh38] Chr9:117005854 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4079C>T (p.Pro1360Leu) | single nucleotide variant | not provided [RCV002172337] | Chr9:114288736 [GRCh38] Chr9:117051016 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4593T>A (p.Ser1531=) | single nucleotide variant | not provided [RCV002212850] | Chr9:114300078 [GRCh38] Chr9:117062358 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4639-20C>T | single nucleotide variant | not provided [RCV002108770] | Chr9:114300605 [GRCh38] Chr9:117062885 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4881T>C (p.Asp1627=) | single nucleotide variant | not provided [RCV002195619] | Chr9:114304616 [GRCh38] Chr9:117066896 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.947G>A (p.Gly316Asp) | single nucleotide variant | Inborn genetic diseases [RCV002561652]|not provided [RCV002212992] | Chr9:114168502 [GRCh38] Chr9:116930782 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.2244A>G (p.Gly748=) | single nucleotide variant | not provided [RCV002114483] | Chr9:114206272 [GRCh38] Chr9:116968552 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3142-16T>C | single nucleotide variant | not provided [RCV002213175] | Chr9:114258525 [GRCh38] Chr9:117020805 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1782G>C (p.Pro594=) | single nucleotide variant | not provided [RCV002214722] | Chr9:114169337 [GRCh38] Chr9:116931617 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5178T>C (p.His1726=) | single nucleotide variant | not provided [RCV002173492] | Chr9:114307739 [GRCh38] Chr9:117070019 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1809G>A (p.Arg603=) | single nucleotide variant | not provided [RCV002152891] | Chr9:114169364 [GRCh38] Chr9:116931644 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2931G>A (p.Val977=) | single nucleotide variant | not provided [RCV002191047] | Chr9:114243557 [GRCh38] Chr9:117005837 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4153-14A>G | single nucleotide variant | not provided [RCV002167293] | Chr9:114289228 [GRCh38] Chr9:117051508 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5289C>A (p.Ile1763=) | single nucleotide variant | not provided [RCV002079975] | Chr9:114309331 [GRCh38] Chr9:117071611 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3402G>A (p.Gln1134=) | single nucleotide variant | not provided [RCV002187067] | Chr9:114266573 [GRCh38] Chr9:117028853 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3448-12G>A | single nucleotide variant | not provided [RCV002167338] | Chr9:114267492 [GRCh38] Chr9:117029772 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2679A>G (p.Lys893=) | single nucleotide variant | not provided [RCV002208094] | Chr9:114237667 [GRCh38] Chr9:116999947 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2520+7A>G | single nucleotide variant | not provided [RCV002091163] | Chr9:114231139 [GRCh38] Chr9:116993419 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2224-20C>T | single nucleotide variant | not provided [RCV002130717] | Chr9:114206232 [GRCh38] Chr9:116968512 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.1980T>C (p.Tyr660=) | single nucleotide variant | not provided [RCV002214706] | Chr9:114183039 [GRCh38] Chr9:116945319 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1812C>A (p.Pro604=) | single nucleotide variant | not provided [RCV002076787] | Chr9:114169367 [GRCh38] Chr9:116931647 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4045-9G>A | single nucleotide variant | not provided [RCV002213268] | Chr9:114288693 [GRCh38] Chr9:117050973 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4682G>A (p.Arg1561Gln) | single nucleotide variant | Inborn genetic diseases [RCV003365692]|not provided [RCV002096639] | Chr9:114300668 [GRCh38] Chr9:117062948 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.3772-17C>A | single nucleotide variant | not provided [RCV002134312] | Chr9:114282440 [GRCh38] Chr9:117044720 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3969T>C (p.Pro1323=) | single nucleotide variant | not provided [RCV002152904] | Chr9:114284759 [GRCh38] Chr9:117047039 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1050T>G (p.Pro350=) | single nucleotide variant | not provided [RCV002106799] | Chr9:114168605 [GRCh38] Chr9:116930885 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4452A>G (p.Gly1484=) | single nucleotide variant | not provided [RCV002074991] | Chr9:114290893 [GRCh38] Chr9:117053173 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3474G>C (p.Pro1158=) | single nucleotide variant | not provided [RCV002144878] | Chr9:114267530 [GRCh38] Chr9:117029810 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3771+10C>G | single nucleotide variant | not provided [RCV002130872] | Chr9:114282340 [GRCh38] Chr9:117044620 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4347G>A (p.Arg1449=) | single nucleotide variant | not provided [RCV002213390] | Chr9:114290310 [GRCh38] Chr9:117052590 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.321C>T (p.His107=) | single nucleotide variant | not provided [RCV002150793] | Chr9:114167876 [GRCh38] Chr9:116930156 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3609+10C>G | single nucleotide variant | not provided [RCV002096761] | Chr9:114270791 [GRCh38] Chr9:117033071 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4779C>T (p.Ser1593=) | single nucleotide variant | not provided [RCV002124440] | Chr9:114301307 [GRCh38] Chr9:117063587 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2172G>A (p.Gly724=) | single nucleotide variant | not provided [RCV002169394] | Chr9:114205761 [GRCh38] Chr9:116968041 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3006C>T (p.Val1002=) | single nucleotide variant | not provided [RCV002094214] | Chr9:114250641 [GRCh38] Chr9:117012921 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4584+10C>T | single nucleotide variant | not provided [RCV002173768] | Chr9:114292220 [GRCh38] Chr9:117054500 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2835+20T>A | single nucleotide variant | not provided [RCV002115987] | Chr9:114240507 [GRCh38] Chr9:117002787 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.258G>C (p.Thr86=) | single nucleotide variant | not provided [RCV002213441] | Chr9:114167813 [GRCh38] Chr9:116930093 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2935-16C>T | single nucleotide variant | not provided [RCV002196238] | Chr9:114245850 [GRCh38] Chr9:117008130 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3087+20C>T | single nucleotide variant | not provided [RCV002080412] | Chr9:114252666 [GRCh38] Chr9:117014946 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5355C>A (p.Ala1785=) | single nucleotide variant | not provided [RCV002213182] | Chr9:114309397 [GRCh38] Chr9:117071677 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1921C>T (p.Leu641=) | single nucleotide variant | not provided [RCV002088673] | Chr9:114178303 [GRCh38] Chr9:116940583 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4938+8C>T | single nucleotide variant | not provided [RCV002169611] | Chr9:114304681 [GRCh38] Chr9:117066961 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5108-10C>T | single nucleotide variant | not provided [RCV002170797] | Chr9:114307659 [GRCh38] Chr9:117069939 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5218-8C>T | single nucleotide variant | not provided [RCV002212298] | Chr9:114309252 [GRCh38] Chr9:117071532 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.240C>A (p.Ala80=) | single nucleotide variant | not provided [RCV002134663] | Chr9:114167795 [GRCh38] Chr9:116930075 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.865A>C (p.Arg289=) | single nucleotide variant | not provided [RCV002193468] | Chr9:114168420 [GRCh38] Chr9:116930700 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1722G>A (p.Arg574=) | single nucleotide variant | not provided [RCV002087475] | Chr9:114169277 [GRCh38] Chr9:116931557 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2444C>T (p.Pro815Leu) | single nucleotide variant | not provided [RCV002172618] | Chr9:114222245 [GRCh38] Chr9:116984525 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2370G>A (p.Gly790=) | single nucleotide variant | not provided [RCV002172436] | Chr9:114219793 [GRCh38] Chr9:116982073 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4752C>G (p.Leu1584=) | single nucleotide variant | not provided [RCV002116692] | Chr9:114301122 [GRCh38] Chr9:117063402 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5097G>A (p.Lys1699=) | single nucleotide variant | not provided [RCV002088894] | Chr9:114306678 [GRCh38] Chr9:117068958 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2169+20C>T | single nucleotide variant | not provided [RCV002169834] | Chr9:114205166 [GRCh38] Chr9:116967446 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.300G>A (p.Leu100=) | single nucleotide variant | not provided [RCV002094383] | Chr9:114167855 [GRCh38] Chr9:116930135 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2836-9C>T | single nucleotide variant | not provided [RCV002210628] | Chr9:114242178 [GRCh38] Chr9:117004458 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1764G>T (p.Pro588=) | single nucleotide variant | not provided [RCV002212451] | Chr9:114169319 [GRCh38] Chr9:116931599 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2511G>A (p.Lys837=) | single nucleotide variant | not provided [RCV002075909] | Chr9:114231123 [GRCh38] Chr9:116993403 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3876A>G (p.Pro1292=) | single nucleotide variant | not provided [RCV002194548] | Chr9:114282561 [GRCh38] Chr9:117044841 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5207C>T (p.Thr1736Met) | single nucleotide variant | not provided [RCV002093959] | Chr9:114307768 [GRCh38] Chr9:117070048 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3250-18G>A | single nucleotide variant | not provided [RCV002150895] | Chr9:114264906 [GRCh38] Chr9:117027186 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.2125-9C>A | single nucleotide variant | not provided [RCV002155725] | Chr9:114205093 [GRCh38] Chr9:116967373 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1909-13G>C | single nucleotide variant | not provided [RCV002135379] | Chr9:114178278 [GRCh38] Chr9:116940558 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.723G>C (p.Thr241=) | single nucleotide variant | not provided [RCV002099819] | Chr9:114168278 [GRCh38] Chr9:116930558 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3474G>A (p.Pro1158=) | single nucleotide variant | not provided [RCV002117621] | Chr9:114267530 [GRCh38] Chr9:117029810 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2442C>G (p.Gly814=) | single nucleotide variant | not provided [RCV002119404] | Chr9:114222243 [GRCh38] Chr9:116984523 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3880-5T>C | single nucleotide variant | not provided [RCV002175444] | Chr9:114283704 [GRCh38] Chr9:117045984 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.777C>A (p.Thr259=) | single nucleotide variant | not provided [RCV002177193] | Chr9:114168332 [GRCh38] Chr9:116930612 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.420G>T (p.Gly140=) | single nucleotide variant | not provided [RCV002119684] | Chr9:114167975 [GRCh38] Chr9:116930255 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4335G>C (p.Gly1445=) | single nucleotide variant | not provided [RCV002220470] | Chr9:114290298 [GRCh38] Chr9:117052578 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4152+14C>T | single nucleotide variant | not provided [RCV002118210] | Chr9:114288981 [GRCh38] Chr9:117051261 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3249+9C>T | single nucleotide variant | not provided [RCV002198579] | Chr9:114264417 [GRCh38] Chr9:117026697 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.863C>A (p.Pro288His) | single nucleotide variant | not provided [RCV002204402] | Chr9:114168418 [GRCh38] Chr9:116930698 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1909-6C>T | single nucleotide variant | not provided [RCV002141889] | Chr9:114178285 [GRCh38] Chr9:116940565 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3987+9T>A | single nucleotide variant | not provided [RCV002120529] | Chr9:114284786 [GRCh38] Chr9:117047066 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2070+14G>A | single nucleotide variant | not provided [RCV002200915] | Chr9:114194471 [GRCh38] Chr9:116956751 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2934+9del | deletion | not provided [RCV002139039] | Chr9:114243569 [GRCh38] Chr9:117005849 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4207-10G>C | single nucleotide variant | not provided [RCV002154064] | Chr9:114290048 [GRCh38] Chr9:117052328 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2935-8C>T | single nucleotide variant | not provided [RCV002083401] | Chr9:114245858 [GRCh38] Chr9:117008138 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5535A>G (p.Ser1845=) | single nucleotide variant | not provided [RCV002163324] | Chr9:114310647 [GRCh38] Chr9:117072927 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3126A>G (p.Gly1042=) | single nucleotide variant | not provided [RCV002137554] | Chr9:114252917 [GRCh38] Chr9:117015197 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2781+13C>T | single nucleotide variant | not provided [RCV002117779] | Chr9:114240286 [GRCh38] Chr9:117002566 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3033+17G>A | single nucleotide variant | not provided [RCV002181403] | Chr9:114250685 [GRCh38] Chr9:117012965 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4752C>T (p.Leu1584=) | single nucleotide variant | not provided [RCV002143171] | Chr9:114301122 [GRCh38] Chr9:117063402 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2235A>G (p.Gly745=) | single nucleotide variant | not provided [RCV002158241] | Chr9:114206263 [GRCh38] Chr9:116968543 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4792-4C>G | single nucleotide variant | not provided [RCV002163673] | Chr9:114301441 [GRCh38] Chr9:117063721 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3064G>A (p.Val1022Met) | single nucleotide variant | not provided [RCV002100462] | Chr9:114252623 [GRCh38] Chr9:117014903 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4692T>C (p.Pro1564=) | single nucleotide variant | not provided [RCV002163793] | Chr9:114300678 [GRCh38] Chr9:117062958 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5529T>C (p.Pro1843=) | single nucleotide variant | not provided [RCV002137992] | Chr9:114310641 [GRCh38] Chr9:117072921 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2728-18C>T | single nucleotide variant | not provided [RCV002120186] | Chr9:114240202 [GRCh38] Chr9:117002482 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3196-20G>A | single nucleotide variant | not provided [RCV002102680] | Chr9:114264335 [GRCh38] Chr9:117026615 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1803C>T (p.Ser601=) | single nucleotide variant | not provided [RCV002164111] | Chr9:114169358 [GRCh38] Chr9:116931638 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4904C>T (p.Thr1635Met) | single nucleotide variant | not provided [RCV002101111] | Chr9:114304639 [GRCh38] Chr9:117066919 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2467-5C>T | single nucleotide variant | not provided [RCV002101115] | Chr9:114231074 [GRCh38] Chr9:116993354 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4515C>G (p.Gly1505=) | single nucleotide variant | not provided [RCV002164358] | Chr9:114292141 [GRCh38] Chr9:117054421 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.62+9G>A | single nucleotide variant | not provided [RCV002099265] | Chr9:114156021 [GRCh38] Chr9:116918301 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4917C>T (p.Thr1639=) | single nucleotide variant | not provided [RCV002155223] | Chr9:114304652 [GRCh38] Chr9:117066932 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1815G>C (p.Thr605=) | single nucleotide variant | not provided [RCV002164608] | Chr9:114169370 [GRCh38] Chr9:116931650 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.133+17T>C | single nucleotide variant | not provided [RCV002101546] | Chr9:114162802 [GRCh38] Chr9:116925082 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4644G>T (p.Pro1548=) | single nucleotide variant | not provided [RCV002162486] | Chr9:114300630 [GRCh38] Chr9:117062910 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3990G>A (p.Gly1330=) | single nucleotide variant | not provided [RCV002157533] | Chr9:114288457 [GRCh38] Chr9:117050737 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5295C>A (p.Ile1765=) | single nucleotide variant | not provided [RCV002176973] | Chr9:114309337 [GRCh38] Chr9:117071617 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4939-8C>T | single nucleotide variant | not provided [RCV002135455] | Chr9:114306512 [GRCh38] Chr9:117068792 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2224-19T>G | single nucleotide variant | not provided [RCV002159125] | Chr9:114206233 [GRCh38] Chr9:116968513 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.354C>T (p.Arg118=) | single nucleotide variant | not provided [RCV002099917] | Chr9:114167909 [GRCh38] Chr9:116930189 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.134-17T>C | single nucleotide variant | not provided [RCV002220505] | Chr9:114167672 [GRCh38] Chr9:116929952 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4203A>C (p.Ala1401=) | single nucleotide variant | not provided [RCV002201785] | Chr9:114289292 [GRCh38] Chr9:117051572 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5211C>T (p.Ala1737=) | single nucleotide variant | not provided [RCV002182651] | Chr9:114307772 [GRCh38] Chr9:117070052 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3651G>A (p.Glu1217=) | single nucleotide variant | not provided [RCV002182674] | Chr9:114275702 [GRCh38] Chr9:117037982 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2568T>C (p.Gly856=) | single nucleotide variant | not provided [RCV002216908] | Chr9:114235601 [GRCh38] Chr9:116997881 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5217+12C>T | single nucleotide variant | not provided [RCV002100313] | Chr9:114307790 [GRCh38] Chr9:117070070 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1524A>C (p.Val508=) | single nucleotide variant | not provided [RCV002217109] | Chr9:114169079 [GRCh38] Chr9:116931359 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4206+12G>A | single nucleotide variant | not provided [RCV002120114] | Chr9:114289307 [GRCh38] Chr9:117051587 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.5370C>G (p.Ala1790=) | single nucleotide variant | not provided [RCV002083798] | Chr9:114309412 [GRCh38] Chr9:117071692 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4464C>T (p.Pro1488=) | single nucleotide variant | not provided [RCV002120084] | Chr9:114290905 [GRCh38] Chr9:117053185 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4206+14G>A | single nucleotide variant | not provided [RCV002182910] | Chr9:114289309 [GRCh38] Chr9:117051589 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3393+17T>C | single nucleotide variant | not provided [RCV002217145] | Chr9:114265492 [GRCh38] Chr9:117027772 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1545C>T (p.Ser515=) | single nucleotide variant | not provided [RCV002198464] | Chr9:114169100 [GRCh38] Chr9:116931380 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5052G>A (p.Glu1684=) | single nucleotide variant | not provided [RCV002154682] | Chr9:114306633 [GRCh38] Chr9:117068913 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.363A>G (p.Lys121=) | single nucleotide variant | not provided [RCV002139697] | Chr9:114167918 [GRCh38] Chr9:116930198 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.501A>G (p.Thr167=) | single nucleotide variant | not provided [RCV002100544] | Chr9:114168056 [GRCh38] Chr9:116930336 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2580T>A (p.Val860=) | single nucleotide variant | not provided [RCV002183007] | Chr9:114235613 [GRCh38] Chr9:116997893 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1884A>T (p.Gly628=) | single nucleotide variant | not provided [RCV002161713] | Chr9:114169439 [GRCh38] Chr9:116931719 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5010C>T (p.Ser1670=) | single nucleotide variant | not provided [RCV002203780] | Chr9:114306591 [GRCh38] Chr9:117068871 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.423C>T (p.Ser141=) | single nucleotide variant | not provided [RCV002162206] | Chr9:114167978 [GRCh38] Chr9:116930258 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.912C>T (p.Ser304=) | single nucleotide variant | not provided [RCV002141638] | Chr9:114168467 [GRCh38] Chr9:116930747 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3394-18TGTC[4] | microsatellite | not provided [RCV002155515] | Chr9:114266546..114266547 [GRCh38] Chr9:117028826..117028827 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3988-4A>G | single nucleotide variant | not provided [RCV002199292] | Chr9:114288451 [GRCh38] Chr9:117050731 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.732C>A (p.Ser244=) | single nucleotide variant | not provided [RCV002201325] | Chr9:114168287 [GRCh38] Chr9:116930567 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.318C>T (p.Ser106=) | single nucleotide variant | not provided [RCV002137321] | Chr9:114167873 [GRCh38] Chr9:116930153 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3153A>C (p.Gly1051=) | single nucleotide variant | not provided [RCV002137101] | Chr9:114258552 [GRCh38] Chr9:117020832 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.888G>A (p.Thr296=) | single nucleotide variant | not provided [RCV002119561] | Chr9:114168443 [GRCh38] Chr9:116930723 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2323-10T>C | single nucleotide variant | not provided [RCV002159314] | Chr9:114210972 [GRCh38] Chr9:116973252 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4756-15C>T | single nucleotide variant | not provided [RCV002218724] | Chr9:114301269 [GRCh38] Chr9:117063549 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1104C>T (p.Leu368=) | single nucleotide variant | not provided [RCV002081790] | Chr9:114168659 [GRCh38] Chr9:116930939 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5107+18C>T | single nucleotide variant | not provided [RCV002083757] | Chr9:114306706 [GRCh38] Chr9:117068986 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2553G>A (p.Leu851=) | single nucleotide variant | not provided [RCV002158408] | Chr9:114231854 [GRCh38] Chr9:116994134 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3996G>A (p.Gln1332=) | single nucleotide variant | not provided [RCV002177845] | Chr9:114288463 [GRCh38] Chr9:117050743 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2881-9C>T | single nucleotide variant | not provided [RCV002177595] | Chr9:114243498 [GRCh38] Chr9:117005778 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4551A>G (p.Gly1517=) | single nucleotide variant | not provided [RCV002175985] | Chr9:114292177 [GRCh38] Chr9:117054457 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3258A>G (p.Pro1086=) | single nucleotide variant | not provided [RCV002139738] | Chr9:114264932 [GRCh38] Chr9:117027212 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1665C>T (p.Val555=) | single nucleotide variant | not provided [RCV002154835] | Chr9:114169220 [GRCh38] Chr9:116931500 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1179A>G (p.Pro393=) | single nucleotide variant | not provided [RCV002159964] | Chr9:114168734 [GRCh38] Chr9:116931014 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3556-9del | deletion | not provided [RCV002141864] | Chr9:114270718 [GRCh38] Chr9:117032998 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4020del (p.Pro1342fs) | deletion | Steel syndrome [RCV002226938] | Chr9:114288484 [GRCh38] Chr9:117050764 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2620-18G>C | single nucleotide variant | not provided [RCV002102937] | Chr9:114236963 [GRCh38] Chr9:116999243 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.4285C>A (p.Arg1429=) | single nucleotide variant | not provided [RCV002101271] | Chr9:114290248 [GRCh38] Chr9:117052528 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3772-7G>C | single nucleotide variant | not provided [RCV002204719] | Chr9:114282450 [GRCh38] Chr9:117044730 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2178A>G (p.Pro726=) | single nucleotide variant | not provided [RCV002204456] | Chr9:114205767 [GRCh38] Chr9:116968047 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.663G>C (p.Val221=) | single nucleotide variant | not provided [RCV002159244] | Chr9:114168218 [GRCh38] Chr9:116930498 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.414C>T (p.His138=) | single nucleotide variant | not provided [RCV002163392] | Chr9:114167969 [GRCh38] Chr9:116930249 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.584G>T (p.Gly195Val) | single nucleotide variant | not provided [RCV003114858] | Chr9:114168139 [GRCh38] Chr9:116930419 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1915C>G (p.Pro639Ala) | single nucleotide variant | not provided [RCV003118045] | Chr9:114178297 [GRCh38] Chr9:116940577 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3321G>T (p.Leu1107Phe) | single nucleotide variant | not provided [RCV003114948] | Chr9:114265092 [GRCh38] Chr9:117027372 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3879+19G>C | single nucleotide variant | not provided [RCV003115542] | Chr9:114282583 [GRCh38] Chr9:117044863 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2367+7del | deletion | not provided [RCV003117331] | Chr9:114211033 [GRCh38] Chr9:116973313 [GRCh37] Chr9:9q32 |
likely benign |
NC_000009.11:g.(?_116037910)_(116993432_?)dup | duplication | not provided [RCV003123074] | Chr9:116037910..116993432 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1166A>G (p.Gln389Arg) | single nucleotide variant | not provided [RCV003118927] | Chr9:114168721 [GRCh38] Chr9:116931001 [GRCh37] Chr9:9q32 |
uncertain significance |
NC_000009.11:g.(?_117037921)_(117072975_?)dup | duplication | not provided [RCV003122913] | Chr9:117037921..117072975 [GRCh37] Chr9:9q32 |
uncertain significance |
NC_000009.11:g.(?_117046993)_(117072977_?)dup | duplication | not provided [RCV003122914] | Chr9:117046993..117072977 [GRCh37] Chr9:9q32 |
uncertain significance |
NC_000009.11:g.(?_116917341)_(116918270_?)del | deletion | not provided [RCV003122915] | Chr9:116917341..116918270 [GRCh37] Chr9:9q32 |
pathogenic |
NC_000009.11:g.(?_117050715)_(117072975_?)dup | duplication | not provided [RCV003122916] | Chr9:117050715..117072975 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3536A>G (p.Gln1179Arg) | single nucleotide variant | not provided [RCV003120099] | Chr9:114269275 [GRCh38] Chr9:117031555 [GRCh37] Chr9:9q32 |
uncertain significance |
GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3 | copy number gain | See cases [RCV002292402] | Chr9:203861..131603223 [GRCh37] Chr9:9p24.3-q34.11 |
pathogenic |
NM_032888.4(COL27A1):c.5558A>C (p.Glu1853Ala) | single nucleotide variant | Inborn genetic diseases [RCV003299768] | Chr9:114310670 [GRCh38] Chr9:117072950 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.211del (p.Gln71fs) | deletion | Steel syndrome [RCV002472215] | Chr9:114167765 [GRCh38] Chr9:116930045 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4854del (p.Gly1620fs) | deletion | Steel syndrome [RCV002465079] | Chr9:114302090 [GRCh38] Chr9:117064370 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.1082C>A (p.Ala361Asp) | single nucleotide variant | Inborn genetic diseases [RCV003288242] | Chr9:114168637 [GRCh38] Chr9:116930917 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.496C>T (p.Arg166Cys) | single nucleotide variant | not provided [RCV003235857] | Chr9:114168051 [GRCh38] Chr9:116930331 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4922G>C (p.Gly1641Ala) | single nucleotide variant | not provided [RCV002298154] | Chr9:114304657 [GRCh38] Chr9:117066937 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4935A>G (p.Pro1645=) | single nucleotide variant | not provided [RCV002838693] | Chr9:114304670 [GRCh38] Chr9:117066950 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4596C>A (p.Gly1532=) | single nucleotide variant | not provided [RCV002774870] | Chr9:114300081 [GRCh38] Chr9:117062361 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1575T>A (p.Thr525=) | single nucleotide variant | not provided [RCV002880590] | Chr9:114169130 [GRCh38] Chr9:116931410 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2724C>G (p.Pro908=) | single nucleotide variant | not provided [RCV002880860] | Chr9:114237712 [GRCh38] Chr9:116999992 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3609+2T>A | single nucleotide variant | not provided [RCV003014643] | Chr9:114270783 [GRCh38] Chr9:117033063 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3056C>A (p.Pro1019His) | single nucleotide variant | not provided [RCV002552009] | Chr9:114252615 [GRCh38] Chr9:117014895 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4728C>A (p.Leu1576=) | single nucleotide variant | not provided [RCV002775192] | Chr9:114301098 [GRCh38] Chr9:117063378 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2326C>G (p.Leu776Val) | single nucleotide variant | Inborn genetic diseases [RCV002839625] | Chr9:114210985 [GRCh38] Chr9:116973265 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4929C>G (p.Leu1643=) | single nucleotide variant | not provided [RCV003014515] | Chr9:114304664 [GRCh38] Chr9:117066944 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2489C>T (p.Pro830Leu) | single nucleotide variant | Inborn genetic diseases [RCV002749026] | Chr9:114231101 [GRCh38] Chr9:116993381 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4755G>C (p.Pro1585=) | single nucleotide variant | not provided [RCV003075115] | Chr9:114301125 [GRCh38] Chr9:117063405 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4583C>T (p.Pro1528Leu) | single nucleotide variant | not provided [RCV003075120] | Chr9:114292209 [GRCh38] Chr9:117054489 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.698G>C (p.Arg233Thr) | single nucleotide variant | Inborn genetic diseases [RCV002770258]|not provided [RCV002756577] | Chr9:114168253 [GRCh38] Chr9:116930533 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5484A>C (p.Gln1828His) | single nucleotide variant | Inborn genetic diseases [RCV002657923]|not provided [RCV002636201] | Chr9:114310596 [GRCh38] Chr9:117072876 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4938+3A>G | single nucleotide variant | not provided [RCV002780045] | Chr9:114304676 [GRCh38] Chr9:117066956 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3622G>C (p.Asp1208His) | single nucleotide variant | not provided [RCV003077098] | Chr9:114275673 [GRCh38] Chr9:117037953 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3613G>C (p.Asp1205His) | single nucleotide variant | Inborn genetic diseases [RCV002992095] | Chr9:114275664 [GRCh38] Chr9:117037944 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.47C>T (p.Ala16Val) | single nucleotide variant | not provided [RCV003074253] | Chr9:114155997 [GRCh38] Chr9:116918277 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1663G>C (p.Val555Leu) | single nucleotide variant | not provided [RCV002686123] | Chr9:114169218 [GRCh38] Chr9:116931498 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4167C>G (p.Pro1389=) | single nucleotide variant | not provided [RCV002842864] | Chr9:114289256 [GRCh38] Chr9:117051536 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.353G>A (p.Arg118His) | single nucleotide variant | not provided [RCV003075516] | Chr9:114167908 [GRCh38] Chr9:116930188 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4099-7C>T | single nucleotide variant | not provided [RCV003034737] | Chr9:114288907 [GRCh38] Chr9:117051187 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1853C>T (p.Thr618Met) | single nucleotide variant | not provided [RCV003076870] | Chr9:114169408 [GRCh38] Chr9:116931688 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3033+2T>G | single nucleotide variant | not provided [RCV002819438] | Chr9:114250670 [GRCh38] Chr9:117012950 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2303C>T (p.Pro768Leu) | single nucleotide variant | not provided [RCV002843803] | Chr9:114209709 [GRCh38] Chr9:116971989 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2304A>G (p.Pro768=) | single nucleotide variant | not provided [RCV002617999] | Chr9:114209710 [GRCh38] Chr9:116971990 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3825T>A (p.Pro1275=) | single nucleotide variant | not provided [RCV002947312] | Chr9:114282510 [GRCh38] Chr9:117044790 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3887C>T (p.Pro1296Leu) | single nucleotide variant | not provided [RCV002615714] | Chr9:114283716 [GRCh38] Chr9:117045996 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1269G>T (p.Glu423Asp) | single nucleotide variant | Inborn genetic diseases [RCV002841045] | Chr9:114168824 [GRCh38] Chr9:116931104 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3377del (p.Gly1126fs) | deletion | not provided [RCV002820065] | Chr9:114265457 [GRCh38] Chr9:117027737 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1686A>G (p.Ala562=) | single nucleotide variant | not provided [RCV002862741] | Chr9:114169241 [GRCh38] Chr9:116931521 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4443C>T (p.Gly1481=) | single nucleotide variant | not provided [RCV003017576] | Chr9:114290884 [GRCh38] Chr9:117053164 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4149A>G (p.Gln1383=) | single nucleotide variant | not provided [RCV002863342] | Chr9:114288964 [GRCh38] Chr9:117051244 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3142-1G>A | single nucleotide variant | not provided [RCV002996616] | Chr9:114258540 [GRCh38] Chr9:117020820 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2808G>T (p.Pro936=) | single nucleotide variant | not provided [RCV002838206] | Chr9:114240460 [GRCh38] Chr9:117002740 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1840C>T (p.Leu614=) | single nucleotide variant | not provided [RCV003016479] | Chr9:114169395 [GRCh38] Chr9:116931675 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2868C>T (p.Ala956=) | single nucleotide variant | not provided [RCV002862808] | Chr9:114242219 [GRCh38] Chr9:117004499 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2606T>C (p.Phe869Ser) | single nucleotide variant | Inborn genetic diseases [RCV002837188] | Chr9:114235639 [GRCh38] Chr9:116997919 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3703G>A (p.Val1235Ile) | single nucleotide variant | Inborn genetic diseases [RCV003058789]|not provided [RCV003074071] | Chr9:114275754 [GRCh38] Chr9:117038034 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.4153-12C>A | single nucleotide variant | not provided [RCV003013682] | Chr9:114289230 [GRCh38] Chr9:117051510 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2169+2T>A | single nucleotide variant | not provided [RCV003016467] | Chr9:114205148 [GRCh38] Chr9:116967428 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2268+1G>T | single nucleotide variant | not provided [RCV002862734] | Chr9:114206297 [GRCh38] Chr9:116968577 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.1053G>C (p.Ala351=) | single nucleotide variant | not provided [RCV003012092] | Chr9:114168608 [GRCh38] Chr9:116930888 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1002T>C (p.Asp334=) | single nucleotide variant | not provided [RCV002681562] | Chr9:114168557 [GRCh38] Chr9:116930837 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.769C>T (p.Pro257Ser) | single nucleotide variant | Inborn genetic diseases [RCV002775687]|not provided [RCV002800370] | Chr9:114168324 [GRCh38] Chr9:116930604 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2917G>A (p.Gly973Ser) | single nucleotide variant | Inborn genetic diseases [RCV002727361] | Chr9:114243543 [GRCh38] Chr9:117005823 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4797G>T (p.Leu1599Phe) | single nucleotide variant | not provided [RCV002775852] | Chr9:114301450 [GRCh38] Chr9:117063730 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2207G>C (p.Gly736Ala) | single nucleotide variant | Inborn genetic diseases [RCV002687076] | Chr9:114205796 [GRCh38] Chr9:116968076 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4351G>A (p.Gly1451Arg) | single nucleotide variant | Inborn genetic diseases [RCV003065220]|not provided [RCV003074247] | Chr9:114290314 [GRCh38] Chr9:117052594 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.533G>A (p.Arg178Gln) | single nucleotide variant | not provided [RCV002972327] | Chr9:114168088 [GRCh38] Chr9:116930368 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3597T>C (p.Pro1199=) | single nucleotide variant | not provided [RCV002863380] | Chr9:114270769 [GRCh38] Chr9:117033049 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3129_3130delinsTT (p.Glu1043_Pro1044delinsAspSer) | indel | not provided [RCV002863400] | Chr9:114252920..114252921 [GRCh38] Chr9:117015200..117015201 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3055C>T (p.Pro1019Ser) | single nucleotide variant | not provided [RCV003095579] | Chr9:114252614 [GRCh38] Chr9:117014894 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1908+1G>A | single nucleotide variant | not provided [RCV002838033] | Chr9:114169464 [GRCh38] Chr9:116931744 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.1960C>T (p.Arg654Trp) | single nucleotide variant | not provided [RCV003095846] | Chr9:114178342 [GRCh38] Chr9:116940622 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4905G>T (p.Thr1635=) | single nucleotide variant | not provided [RCV002861802] | Chr9:114304640 [GRCh38] Chr9:117066920 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1814C>T (p.Thr605Met) | single nucleotide variant | Inborn genetic diseases [RCV002982782]|not provided [RCV002995228] | Chr9:114169369 [GRCh38] Chr9:116931649 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4523G>T (p.Gly1508Val) | single nucleotide variant | not provided [RCV002613596] | Chr9:114292149 [GRCh38] Chr9:117054429 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2370G>T (p.Gly790=) | single nucleotide variant | not provided [RCV002756335] | Chr9:114219793 [GRCh38] Chr9:116982073 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.277G>A (p.Ala93Thr) | single nucleotide variant | Inborn genetic diseases [RCV002947404]|not provided [RCV002910209] | Chr9:114167832 [GRCh38] Chr9:116930112 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1551C>T (p.Pro517=) | single nucleotide variant | not provided [RCV002819842] | Chr9:114169106 [GRCh38] Chr9:116931386 [GRCh37] Chr9:9q32 |
likely benign |
NC_000009.12:g.114231822_114231832del | deletion | not provided [RCV003012486] | Chr9:114231821..114231831 [GRCh38] Chr9:116994101..116994111 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3995A>G (p.Gln1332Arg) | single nucleotide variant | not provided [RCV003073679] | Chr9:114288462 [GRCh38] Chr9:117050742 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.114C>T (p.Ser38=) | single nucleotide variant | not provided [RCV002756368] | Chr9:114162766 [GRCh38] Chr9:116925046 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4670T>C (p.Ile1557Thr) | single nucleotide variant | Inborn genetic diseases [RCV002836560] | Chr9:114300656 [GRCh38] Chr9:117062936 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2516T>C (p.Met839Thr) | single nucleotide variant | not provided [RCV002948031] | Chr9:114231128 [GRCh38] Chr9:116993408 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4792-7C>A | single nucleotide variant | not provided [RCV003034800] | Chr9:114301438 [GRCh38] Chr9:117063718 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3294+10G>T | single nucleotide variant | not provided [RCV002618202] | Chr9:114264978 [GRCh38] Chr9:117027258 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3747C>G (p.Gly1249=) | single nucleotide variant | not provided [RCV002862286] | Chr9:114282306 [GRCh38] Chr9:117044586 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4939-16C>T | single nucleotide variant | not provided [RCV003074800] | Chr9:114306504 [GRCh38] Chr9:117068784 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3988-15G>A | single nucleotide variant | not provided [RCV002819085] | Chr9:114288440 [GRCh38] Chr9:117050720 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2807C>T (p.Pro936Leu) | single nucleotide variant | Inborn genetic diseases [RCV003051330]|not provided [RCV003076549] | Chr9:114240459 [GRCh38] Chr9:117002739 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.569C>G (p.Ala190Gly) | single nucleotide variant | not provided [RCV002726666] | Chr9:114168124 [GRCh38] Chr9:116930404 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2782-16G>A | single nucleotide variant | not provided [RCV002889530] | Chr9:114240418 [GRCh38] Chr9:117002698 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4717G>A (p.Val1573Ile) | single nucleotide variant | not provided [RCV002659723] | Chr9:114301087 [GRCh38] Chr9:117063367 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2536G>A (p.Val846Met) | single nucleotide variant | not provided [RCV003079722] | Chr9:114231837 [GRCh38] Chr9:116994117 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1505G>A (p.Arg502Gln) | single nucleotide variant | not provided [RCV002927939] | Chr9:114169060 [GRCh38] Chr9:116931340 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4178C>T (p.Pro1393Leu) | single nucleotide variant | Inborn genetic diseases [RCV003077463]|not provided [RCV003077462] | Chr9:114289267 [GRCh38] Chr9:117051547 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4809+8G>C | single nucleotide variant | not provided [RCV002923601] | Chr9:114301470 [GRCh38] Chr9:117063750 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2670T>C (p.Pro890=) | single nucleotide variant | not provided [RCV003039350] | Chr9:114237031 [GRCh38] Chr9:116999311 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4520G>A (p.Arg1507Gln) | single nucleotide variant | Inborn genetic diseases [RCV003081507]|not provided [RCV003068997] | Chr9:114292146 [GRCh38] Chr9:117054426 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4756-4G>T | single nucleotide variant | not provided [RCV002846840] | Chr9:114301280 [GRCh38] Chr9:117063560 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1497G>T (p.Arg499Ser) | single nucleotide variant | not provided [RCV002786067] | Chr9:114169052 [GRCh38] Chr9:116931332 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1320C>T (p.Thr440=) | single nucleotide variant | not provided [RCV003021849] | Chr9:114168875 [GRCh38] Chr9:116931155 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2264G>A (p.Ser755Asn) | single nucleotide variant | not provided [RCV002622012] | Chr9:114206292 [GRCh38] Chr9:116968572 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3689_3690delinsAT (p.Pro1230His) | indel | not provided [RCV002640640] | Chr9:114275740..114275741 [GRCh38] Chr9:117038020..117038021 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4472T>C (p.Phe1491Ser) | single nucleotide variant | not provided [RCV002571928] | Chr9:114290913 [GRCh38] Chr9:117053193 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4880A>G (p.Asp1627Gly) | single nucleotide variant | not provided [RCV002953561] | Chr9:114304615 [GRCh38] Chr9:117066895 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1518G>T (p.Thr506=) | single nucleotide variant | not provided [RCV002623223] | Chr9:114169073 [GRCh38] Chr9:116931353 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4966C>T (p.Leu1656=) | single nucleotide variant | not provided [RCV002889691] | Chr9:114306547 [GRCh38] Chr9:117068827 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4832G>A (p.Arg1611Gln) | single nucleotide variant | Inborn genetic diseases [RCV003170592]|not provided [RCV002909822] | Chr9:114301704 [GRCh38] Chr9:117063984 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.2836-18C>T | single nucleotide variant | not provided [RCV002761316] | Chr9:114242169 [GRCh38] Chr9:117004449 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2502G>A (p.Pro834=) | single nucleotide variant | not provided [RCV002949668] | Chr9:114231114 [GRCh38] Chr9:116993394 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2796C>A (p.Ala932=) | single nucleotide variant | not provided [RCV003078584] | Chr9:114240448 [GRCh38] Chr9:117002728 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.528G>A (p.Gln176=) | single nucleotide variant | not provided [RCV002889777] | Chr9:114168083 [GRCh38] Chr9:116930363 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3811G>A (p.Val1271Ile) | single nucleotide variant | not provided [RCV002953419] | Chr9:114282496 [GRCh38] Chr9:117044776 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.7G>A (p.Ala3Thr) | single nucleotide variant | Inborn genetic diseases [RCV003171077]|not provided [RCV003081373] | Chr9:114155957 [GRCh38] Chr9:116918237 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4844C>T (p.Pro1615Leu) | single nucleotide variant | not provided [RCV003078902] | Chr9:114301716 [GRCh38] Chr9:117063996 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2161G>A (p.Gly721Arg) | single nucleotide variant | not provided [RCV002638146] | Chr9:114205138 [GRCh38] Chr9:116967418 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.616G>A (p.Ala206Thr) | single nucleotide variant | Inborn genetic diseases [RCV002660052] | Chr9:114168171 [GRCh38] Chr9:116930451 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2620-11A>G | single nucleotide variant | not provided [RCV003077486] | Chr9:114236970 [GRCh38] Chr9:116999250 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1289del (p.Pro430fs) | deletion | not provided [RCV002796536] | Chr9:114168842 [GRCh38] Chr9:116931122 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.418G>A (p.Gly140Arg) | single nucleotide variant | Inborn genetic diseases [RCV003167942]|not provided [RCV002909695] | Chr9:114167973 [GRCh38] Chr9:116930253 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.408C>G (p.Val136=) | single nucleotide variant | not provided [RCV002620064] | Chr9:114167963 [GRCh38] Chr9:116930243 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3354C>T (p.Pro1118=) | single nucleotide variant | not provided [RCV002760864] | Chr9:114265436 [GRCh38] Chr9:117027716 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1290G>C (p.Pro430=) | single nucleotide variant | not provided [RCV003077655] | Chr9:114168845 [GRCh38] Chr9:116931125 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5157G>A (p.Glu1719=) | single nucleotide variant | not provided [RCV003038025] | Chr9:114307718 [GRCh38] Chr9:117069998 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2536G>T (p.Val846Leu) | single nucleotide variant | not provided [RCV002591736] | Chr9:114231837 [GRCh38] Chr9:116994117 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2781+15A>C | single nucleotide variant | not provided [RCV002619178] | Chr9:114240288 [GRCh38] Chr9:117002568 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4193C>A (p.Ser1398Ter) | single nucleotide variant | not provided [RCV002868041] | Chr9:114289282 [GRCh38] Chr9:117051562 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4939-17C>T | single nucleotide variant | not provided [RCV002705471] | Chr9:114306503 [GRCh38] Chr9:117068783 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3209C>T (p.Pro1070Leu) | single nucleotide variant | not provided [RCV002999478] | Chr9:114264368 [GRCh38] Chr9:117026648 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2360G>A (p.Gly787Asp) | single nucleotide variant | Inborn genetic diseases [RCV002950286] | Chr9:114211019 [GRCh38] Chr9:116973299 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.770C>A (p.Pro257His) | single nucleotide variant | Inborn genetic diseases [RCV002895808]|not provided [RCV002912984] | Chr9:114168325 [GRCh38] Chr9:116930605 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4122C>G (p.Leu1374=) | single nucleotide variant | not provided [RCV003038151] | Chr9:114288937 [GRCh38] Chr9:117051217 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2124+3A>T | single nucleotide variant | not provided [RCV002847679] | Chr9:114196015 [GRCh38] Chr9:116958295 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4299G>A (p.Gly1433=) | single nucleotide variant | not provided [RCV003037835] | Chr9:114290262 [GRCh38] Chr9:117052542 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3579C>T (p.Asp1193=) | single nucleotide variant | not provided [RCV003080190] | Chr9:114270751 [GRCh38] Chr9:117033031 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1275C>T (p.Pro425=) | single nucleotide variant | not provided [RCV003037956] | Chr9:114168830 [GRCh38] Chr9:116931110 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2841T>G (p.Asp947Glu) | single nucleotide variant | Inborn genetic diseases [RCV002869831] | Chr9:114242192 [GRCh38] Chr9:117004472 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4639-14T>A | single nucleotide variant | not provided [RCV003077522] | Chr9:114300611 [GRCh38] Chr9:117062891 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3083C>T (p.Ser1028Leu) | single nucleotide variant | not provided [RCV002637307] | Chr9:114252642 [GRCh38] Chr9:117014922 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1979A>T (p.Tyr660Phe) | single nucleotide variant | Inborn genetic diseases [RCV002822256] | Chr9:114183038 [GRCh38] Chr9:116945318 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2521-4G>A | single nucleotide variant | not provided [RCV003079699] | Chr9:114231818 [GRCh38] Chr9:116994098 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3906A>G (p.Gln1302=) | single nucleotide variant | not provided [RCV002569751] | Chr9:114283735 [GRCh38] Chr9:117046015 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4873C>T (p.Gln1625Ter) | single nucleotide variant | not provided [RCV003077622] | Chr9:114304608 [GRCh38] Chr9:117066888 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.883G>A (p.Ala295Thr) | single nucleotide variant | not provided [RCV002637075] | Chr9:114168438 [GRCh38] Chr9:116930718 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4261-4C>T | single nucleotide variant | not provided [RCV002760390] | Chr9:114290220 [GRCh38] Chr9:117052500 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1963-6_1963-3del | deletion | not provided [RCV002797072] | Chr9:114183014..114183017 [GRCh38] Chr9:116945294..116945297 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1017C>G (p.Ala339=) | single nucleotide variant | not provided [RCV003038531] | Chr9:114168572 [GRCh38] Chr9:116930852 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1488T>C (p.Gly496=) | single nucleotide variant | not provided [RCV002639540] | Chr9:114169043 [GRCh38] Chr9:116931323 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4069C>T (p.Arg1357Cys) | single nucleotide variant | not provided [RCV002637513] | Chr9:114288726 [GRCh38] Chr9:117051006 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3041G>A (p.Arg1014His) | single nucleotide variant | not provided [RCV002659718] | Chr9:114252600 [GRCh38] Chr9:117014880 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1329A>G (p.Leu443=) | single nucleotide variant | not provided [RCV002621627] | Chr9:114168884 [GRCh38] Chr9:116931164 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4741C>A (p.Pro1581Thr) | single nucleotide variant | not provided [RCV003053137] | Chr9:114301111 [GRCh38] Chr9:117063391 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4729G>T (p.Gly1577Ter) | single nucleotide variant | not provided [RCV002871090] | Chr9:114301099 [GRCh38] Chr9:117063379 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1254C>G (p.Val418=) | single nucleotide variant | not provided [RCV003000044] | Chr9:114168809 [GRCh38] Chr9:116931089 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4263C>T (p.Gly1421=) | single nucleotide variant | not provided [RCV002760984] | Chr9:114290226 [GRCh38] Chr9:117052506 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1412C>T (p.Pro471Leu) | single nucleotide variant | Inborn genetic diseases [RCV003086604]|not provided [RCV003100174] | Chr9:114168967 [GRCh38] Chr9:116931247 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4672C>T (p.Gln1558Ter) | single nucleotide variant | not provided [RCV002952620] | Chr9:114300658 [GRCh38] Chr9:117062938 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4168C>A (p.Arg1390=) | single nucleotide variant | not provided [RCV002824992] | Chr9:114289257 [GRCh38] Chr9:117051537 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5125C>A (p.Pro1709Thr) | single nucleotide variant | not provided [RCV002591108] | Chr9:114307686 [GRCh38] Chr9:117069966 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.994G>A (p.Ala332Thr) | single nucleotide variant | not provided [RCV003080086] | Chr9:114168549 [GRCh38] Chr9:116930829 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2461C>T (p.Leu821Phe) | single nucleotide variant | not provided [RCV003080500] | Chr9:114222262 [GRCh38] Chr9:116984542 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1920GCTACCTGG[1] (p.641LPG[1]) | microsatellite | not provided [RCV002913481] | Chr9:114178297..114178305 [GRCh38] Chr9:116940577..116940585 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2422-17TC[2] | microsatellite | not provided [RCV003080514] | Chr9:114222206..114222209 [GRCh38] Chr9:116984486..116984489 [GRCh37] Chr9:9q32 |
likely benign|uncertain significance |
NM_032888.4(COL27A1):c.4538C>T (p.Thr1513Met) | single nucleotide variant | not provided [RCV003053008] | Chr9:114292164 [GRCh38] Chr9:117054444 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4974G>A (p.Gln1658=) | single nucleotide variant | not provided [RCV002639699] | Chr9:114306555 [GRCh38] Chr9:117068835 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3553C>T (p.Arg1185Trp) | single nucleotide variant | not provided [RCV003002337] | Chr9:114269292 [GRCh38] Chr9:117031572 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.279C>G (p.Ala93=) | single nucleotide variant | not provided [RCV002824859] | Chr9:114167834 [GRCh38] Chr9:116930114 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4193C>G (p.Ser1398Trp) | single nucleotide variant | not provided [RCV003078217] | Chr9:114289282 [GRCh38] Chr9:117051562 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1567G>A (p.Val523Ile) | single nucleotide variant | Inborn genetic diseases [RCV003053020]|not provided [RCV003053021] | Chr9:114169122 [GRCh38] Chr9:116931402 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2016+2_2016+3del | deletion | not provided [RCV002889378] | Chr9:114183076..114183077 [GRCh38] Chr9:116945356..116945357 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.63-3_77del | deletion | not provided [RCV002846715] | Chr9:114162708..114162725 [GRCh38] Chr9:116924988..116925005 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2125-6C>T | single nucleotide variant | not provided [RCV003054505] | Chr9:114205096 [GRCh38] Chr9:116967376 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3340-10G>T | single nucleotide variant | not provided [RCV003100184] | Chr9:114265412 [GRCh38] Chr9:117027692 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5262G>T (p.Leu1754=) | single nucleotide variant | not provided [RCV002846495] | Chr9:114309304 [GRCh38] Chr9:117071584 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.944G>A (p.Gly315Glu) | single nucleotide variant | Inborn genetic diseases [RCV003002705]|not provided [RCV003002704] | Chr9:114168499 [GRCh38] Chr9:116930779 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.63-6C>A | single nucleotide variant | not provided [RCV002867862] | Chr9:114162709 [GRCh38] Chr9:116924989 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2527A>T (p.Met843Leu) | single nucleotide variant | not provided [RCV002886502] | Chr9:114231828 [GRCh38] Chr9:116994108 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1654C>T (p.Arg552Trp) | single nucleotide variant | not provided [RCV002638510] | Chr9:114169209 [GRCh38] Chr9:116931489 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3340-4G>T | single nucleotide variant | not provided [RCV002761128] | Chr9:114265418 [GRCh38] Chr9:117027698 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.39G>A (p.Ala13=) | single nucleotide variant | not provided [RCV002870709] | Chr9:114155989 [GRCh38] Chr9:116918269 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5256G>T (p.Leu1752=) | single nucleotide variant | not provided [RCV003021227] | Chr9:114309298 [GRCh38] Chr9:117071578 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3573G>A (p.Glu1191=) | single nucleotide variant | not provided [RCV003019266] | Chr9:114270745 [GRCh38] Chr9:117033025 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4507C>T (p.Pro1503Ser) | single nucleotide variant | not provided [RCV002620211] | Chr9:114292133 [GRCh38] Chr9:117054413 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4257C>T (p.Val1419=) | single nucleotide variant | not provided [RCV002867681] | Chr9:114290108 [GRCh38] Chr9:117052388 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4946G>C (p.Ser1649Thr) | single nucleotide variant | not provided [RCV003054411] | Chr9:114306527 [GRCh38] Chr9:117068807 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4339C>A (p.Pro1447Thr) | single nucleotide variant | not provided [RCV002619705] | Chr9:114290302 [GRCh38] Chr9:117052582 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1845A>G (p.Ala615=) | single nucleotide variant | not provided [RCV002636382] | Chr9:114169400 [GRCh38] Chr9:116931680 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4929C>A (p.Leu1643=) | single nucleotide variant | not provided [RCV002894883] | Chr9:114304664 [GRCh38] Chr9:117066944 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4465C>A (p.Pro1489Thr) | single nucleotide variant | not provided [RCV002626130] | Chr9:114290906 [GRCh38] Chr9:117053186 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1951C>T (p.Arg651Cys) | single nucleotide variant | Inborn genetic diseases [RCV002702217] | Chr9:114178333 [GRCh38] Chr9:116940613 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5499G>T (p.Leu1833=) | single nucleotide variant | not provided [RCV002890137] | Chr9:114310611 [GRCh38] Chr9:117072891 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1869G>A (p.Leu623=) | single nucleotide variant | not provided [RCV002876744] | Chr9:114169424 [GRCh38] Chr9:116931704 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3294+16G>A | single nucleotide variant | not provided [RCV002893906] | Chr9:114264984 [GRCh38] Chr9:117027264 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4247G>A (p.Arg1416Gln) | single nucleotide variant | not provided [RCV003085932] | Chr9:114290098 [GRCh38] Chr9:117052378 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3249+4C>T | single nucleotide variant | not provided [RCV003086013] | Chr9:114264412 [GRCh38] Chr9:117026692 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.673G>A (p.Ala225Thr) | single nucleotide variant | Inborn genetic diseases [RCV003161742]|not provided [RCV003085825] | Chr9:114168228 [GRCh38] Chr9:116930508 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3868C>T (p.Leu1290=) | single nucleotide variant | not provided [RCV002932240] | Chr9:114282553 [GRCh38] Chr9:117044833 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3864C>T (p.Gly1288=) | single nucleotide variant | not provided [RCV002624123] | Chr9:114282549 [GRCh38] Chr9:117044829 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2324G>T (p.Gly775Val) | single nucleotide variant | Inborn genetic diseases [RCV002958954]|not provided [RCV002958955] | Chr9:114210983 [GRCh38] Chr9:116973263 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3129G>A (p.Glu1043=) | single nucleotide variant | not provided [RCV002894097] | Chr9:114252920 [GRCh38] Chr9:117015200 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4569G>A (p.Gly1523=) | single nucleotide variant | not provided [RCV002597282] | Chr9:114292195 [GRCh38] Chr9:117054475 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1064C>A (p.Pro355Gln) | single nucleotide variant | not provided [RCV002805826] | Chr9:114168619 [GRCh38] Chr9:116930899 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.885C>A (p.Ala295=) | single nucleotide variant | not provided [RCV002918533] | Chr9:114168440 [GRCh38] Chr9:116930720 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2269-2A>G | single nucleotide variant | not provided [RCV002802005] | Chr9:114209673 [GRCh38] Chr9:116971953 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3052G>A (p.Gly1018Arg) | single nucleotide variant | Inborn genetic diseases [RCV002712961] | Chr9:114252611 [GRCh38] Chr9:117014891 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.250G>A (p.Ala84Thr) | single nucleotide variant | Inborn genetic diseases [RCV002919712] | Chr9:114167805 [GRCh38] Chr9:116930085 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2153G>C (p.Gly718Ala) | single nucleotide variant | not provided [RCV002575541] | Chr9:114205130 [GRCh38] Chr9:116967410 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3021C>T (p.Ile1007=) | single nucleotide variant | not provided [RCV002805512] | Chr9:114250656 [GRCh38] Chr9:117012936 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1644G>A (p.Lys548=) | single nucleotide variant | not provided [RCV002576140] | Chr9:114169199 [GRCh38] Chr9:116931479 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.897G>A (p.Lys299=) | single nucleotide variant | not provided [RCV002894351] | Chr9:114168452 [GRCh38] Chr9:116930732 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1154C>T (p.Pro385Leu) | single nucleotide variant | not provided [RCV003084381] | Chr9:114168709 [GRCh38] Chr9:116930989 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5064G>C (p.Arg1688=) | single nucleotide variant | not provided [RCV003040383] | Chr9:114306645 [GRCh38] Chr9:117068925 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1745C>A (p.Pro582His) | single nucleotide variant | not provided [RCV003084463] | Chr9:114169300 [GRCh38] Chr9:116931580 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.215C>T (p.Ser72Leu) | single nucleotide variant | not provided [RCV003056469] | Chr9:114167770 [GRCh38] Chr9:116930050 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5436+9C>G | single nucleotide variant | not provided [RCV003057879] | Chr9:114309487 [GRCh38] Chr9:117071767 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4399C>T (p.Pro1467Ser) | single nucleotide variant | Inborn genetic diseases [RCV002826112] | Chr9:114290840 [GRCh38] Chr9:117053120 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.199G>A (p.Val67Ile) | single nucleotide variant | not provided [RCV002643224] | Chr9:114167754 [GRCh38] Chr9:116930034 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2159C>T (p.Pro720Leu) | single nucleotide variant | not provided [RCV002624983] | Chr9:114205136 [GRCh38] Chr9:116967416 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1356A>G (p.Lys452=) | single nucleotide variant | not provided [RCV002828702] | Chr9:114168911 [GRCh38] Chr9:116931191 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1020T>C (p.Ser340=) | single nucleotide variant | not provided [RCV002957301] | Chr9:114168575 [GRCh38] Chr9:116930855 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3360C>A (p.Gly1120=) | single nucleotide variant | not provided [RCV002872370] | Chr9:114265442 [GRCh38] Chr9:117027722 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5241C>T (p.Val1747=) | single nucleotide variant | not provided [RCV002917903] | Chr9:114309283 [GRCh38] Chr9:117071563 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5397G>C (p.Gly1799=) | single nucleotide variant | not provided [RCV003005369] | Chr9:114309439 [GRCh38] Chr9:117071719 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5025C>A (p.Ser1675Arg) | single nucleotide variant | not provided [RCV002595828] | Chr9:114306606 [GRCh38] Chr9:117068886 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2929G>A (p.Val977Met) | single nucleotide variant | Inborn genetic diseases [RCV003003814] | Chr9:114243555 [GRCh38] Chr9:117005835 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.574G>A (p.Asp192Asn) | single nucleotide variant | not provided [RCV002643444] | Chr9:114168129 [GRCh38] Chr9:116930409 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4200C>T (p.Gly1400=) | single nucleotide variant | not provided [RCV002624940] | Chr9:114289289 [GRCh38] Chr9:117051569 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.830C>T (p.Pro277Leu) | single nucleotide variant | not provided [RCV002711169] | Chr9:114168385 [GRCh38] Chr9:116930665 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5517C>A (p.Asp1839Glu) | single nucleotide variant | Inborn genetic diseases [RCV002588579]|not provided [RCV002595457] | Chr9:114310629 [GRCh38] Chr9:117072909 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4584+11G>C | single nucleotide variant | not provided [RCV002644548] | Chr9:114292221 [GRCh38] Chr9:117054501 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3950T>C (p.Val1317Ala) | single nucleotide variant | not provided [RCV002829234] | Chr9:114284740 [GRCh38] Chr9:117047020 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5218-16C>T | single nucleotide variant | not provided [RCV002574561] | Chr9:114309244 [GRCh38] Chr9:117071524 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1827T>C (p.Tyr609=) | single nucleotide variant | not provided [RCV002933186] | Chr9:114169382 [GRCh38] Chr9:116931662 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2268+15G>T | single nucleotide variant | not provided [RCV003024825] | Chr9:114206311 [GRCh38] Chr9:116968591 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1699C>T (p.Pro567Ser) | single nucleotide variant | not provided [RCV002829893] | Chr9:114169254 [GRCh38] Chr9:116931534 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2601C>G (p.Pro867=) | single nucleotide variant | not provided [RCV002710127] | Chr9:114235634 [GRCh38] Chr9:116997914 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1388A>G (p.Lys463Arg) | single nucleotide variant | not provided [RCV002851414] | Chr9:114168943 [GRCh38] Chr9:116931223 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3598G>C (p.Asp1200His) | single nucleotide variant | not provided [RCV002574145] | Chr9:114270770 [GRCh38] Chr9:117033050 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.457G>A (p.Asp153Asn) | single nucleotide variant | not provided [RCV003083122] | Chr9:114168012 [GRCh38] Chr9:116930292 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.981G>C (p.Leu327=) | single nucleotide variant | not provided [RCV002872643] | Chr9:114168536 [GRCh38] Chr9:116930816 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1807C>T (p.Arg603Trp) | single nucleotide variant | not provided [RCV002625100] | Chr9:114169362 [GRCh38] Chr9:116931642 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3698dup (p.Gly1234fs) | duplication | not provided [RCV002851888] | Chr9:114275743..114275744 [GRCh38] Chr9:117038023..117038024 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4156C>T (p.His1386Tyr) | single nucleotide variant | not provided [RCV002644378] | Chr9:114289245 [GRCh38] Chr9:117051525 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.322C>T (p.Arg108Trp) | single nucleotide variant | not provided [RCV002663968] | Chr9:114167877 [GRCh38] Chr9:116930157 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3462A>G (p.Ala1154=) | single nucleotide variant | not provided [RCV002957173] | Chr9:114267518 [GRCh38] Chr9:117029798 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.761C>G (p.Ser254Cys) | single nucleotide variant | not provided [RCV002919033] | Chr9:114168316 [GRCh38] Chr9:116930596 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1332T>G (p.Pro444=) | single nucleotide variant | not provided [RCV002871774] | Chr9:114168887 [GRCh38] Chr9:116931167 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4791+8G>A | single nucleotide variant | not provided [RCV002853081] | Chr9:114301327 [GRCh38] Chr9:117063607 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4669A>T (p.Ile1557Phe) | single nucleotide variant | not provided [RCV003058797] | Chr9:114300655 [GRCh38] Chr9:117062935 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4168C>T (p.Arg1390Trp) | single nucleotide variant | not provided [RCV003005330] | Chr9:114289257 [GRCh38] Chr9:117051537 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3419T>C (p.Ile1140Thr) | single nucleotide variant | not provided [RCV002644073] | Chr9:114266590 [GRCh38] Chr9:117028870 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4099-8G>A | single nucleotide variant | not provided [RCV002596354] | Chr9:114288906 [GRCh38] Chr9:117051186 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4958G>A (p.Arg1653Gln) | single nucleotide variant | not provided [RCV002766195] | Chr9:114306539 [GRCh38] Chr9:117068819 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2782-11C>A | single nucleotide variant | not provided [RCV002853116] | Chr9:114240423 [GRCh38] Chr9:117002703 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3195+1G>A | single nucleotide variant | not provided [RCV002894466] | Chr9:114258595 [GRCh38] Chr9:117020875 [GRCh37] Chr9:9q32 |
pathogenic|likely pathogenic |
NM_032888.4(COL27A1):c.1808G>A (p.Arg603Gln) | single nucleotide variant | Inborn genetic diseases [RCV002827790] | Chr9:114169363 [GRCh38] Chr9:116931643 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4658G>T (p.Gly1553Val) | single nucleotide variant | not provided [RCV002851889] | Chr9:114300644 [GRCh38] Chr9:117062924 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4560_4561del (p.Glu1521fs) | deletion | not provided [RCV002830085] | Chr9:114292183..114292184 [GRCh38] Chr9:117054463..117054464 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.570A>C (p.Ala190=) | single nucleotide variant | not provided [RCV002872440] | Chr9:114168125 [GRCh38] Chr9:116930405 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-18C>T | single nucleotide variant | not provided [RCV002625129] | Chr9:114250597 [GRCh38] Chr9:117012877 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4246C>T (p.Arg1416Trp) | single nucleotide variant | Inborn genetic diseases [RCV003294412]|not provided [RCV003058520] | Chr9:114290097 [GRCh38] Chr9:117052377 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2305G>C (p.Gly769Arg) | single nucleotide variant | not provided [RCV002642235] | Chr9:114209711 [GRCh38] Chr9:116971991 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.203T>C (p.Ile68Thr) | single nucleotide variant | Inborn genetic diseases [RCV002767548] | Chr9:114167758 [GRCh38] Chr9:116930038 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2910G>A (p.Gly970=) | single nucleotide variant | not provided [RCV002573042] | Chr9:114243536 [GRCh38] Chr9:117005816 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3375G>A (p.Lys1125=) | single nucleotide variant | not provided [RCV002573873] | Chr9:114265457 [GRCh38] Chr9:117027737 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.18G>A (p.Ala6=) | single nucleotide variant | not provided [RCV002917271] | Chr9:114155968 [GRCh38] Chr9:116918248 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2098G>A (p.Gly700Arg) | single nucleotide variant | not provided [RCV002957341] | Chr9:114195986 [GRCh38] Chr9:116958266 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.230C>T (p.Thr77Met) | single nucleotide variant | not provided [RCV002958100] | Chr9:114167785 [GRCh38] Chr9:116930065 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2935-13T>C | single nucleotide variant | not provided [RCV002954286] | Chr9:114245853 [GRCh38] Chr9:117008133 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.323G>C (p.Arg108Pro) | single nucleotide variant | not provided [RCV002985397] | Chr9:114167878 [GRCh38] Chr9:116930158 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4045-5T>C | single nucleotide variant | not provided [RCV002765834] | Chr9:114288697 [GRCh38] Chr9:117050977 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2268+1G>A | single nucleotide variant | not provided [RCV003023196] | Chr9:114206297 [GRCh38] Chr9:116968577 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2363T>A (p.Met788Lys) | single nucleotide variant | Inborn genetic diseases [RCV002853620] | Chr9:114211022 [GRCh38] Chr9:116973302 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1226C>A (p.Pro409His) | single nucleotide variant | not provided [RCV002954357] | Chr9:114168781 [GRCh38] Chr9:116931061 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4164A>C (p.Gly1388=) | single nucleotide variant | not provided [RCV002985336] | Chr9:114289253 [GRCh38] Chr9:117051533 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.373C>A (p.Gln125Lys) | single nucleotide variant | not provided [RCV002790455] | Chr9:114167928 [GRCh38] Chr9:116930208 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.134-7C>T | single nucleotide variant | not provided [RCV002632718] | Chr9:114167682 [GRCh38] Chr9:116929962 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2589G>T (p.Val863=) | single nucleotide variant | not provided [RCV002602184] | Chr9:114235622 [GRCh38] Chr9:116997902 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1046G>A (p.Arg349His) | single nucleotide variant | Inborn genetic diseases [RCV002602741]|not provided [RCV002602740] | Chr9:114168601 [GRCh38] Chr9:116930881 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3849T>C (p.Pro1283=) | single nucleotide variant | not provided [RCV003043950] | Chr9:114282534 [GRCh38] Chr9:117044814 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.426G>A (p.Arg142=) | single nucleotide variant | not provided [RCV002676546] | Chr9:114167981 [GRCh38] Chr9:116930261 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5040G>A (p.Leu1680=) | single nucleotide variant | not provided [RCV002791891] | Chr9:114306621 [GRCh38] Chr9:117068901 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4713C>A (p.Gly1571=) | single nucleotide variant | not provided [RCV002633005] | Chr9:114301083 [GRCh38] Chr9:117063363 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4509C>T (p.Pro1503=) | single nucleotide variant | not provided [RCV002746711] | Chr9:114292135 [GRCh38] Chr9:117054415 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2782-4C>T | single nucleotide variant | not provided [RCV003063812] | Chr9:114240430 [GRCh38] Chr9:117002710 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.395C>T (p.Pro132Leu) | single nucleotide variant | not provided [RCV002582055] | Chr9:114167950 [GRCh38] Chr9:116930230 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1063C>T (p.Pro355Ser) | single nucleotide variant | not provided [RCV003090212] | Chr9:114168618 [GRCh38] Chr9:116930898 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1728C>T (p.Ser576=) | single nucleotide variant | not provided [RCV002633072] | Chr9:114169283 [GRCh38] Chr9:116931563 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5293A>C (p.Ile1765Leu) | single nucleotide variant | not provided [RCV002963180] | Chr9:114309335 [GRCh38] Chr9:117071615 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4210C>A (p.Pro1404Thr) | single nucleotide variant | not provided [RCV002720447] | Chr9:114290061 [GRCh38] Chr9:117052341 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4687C>T (p.Pro1563Ser) | single nucleotide variant | not provided [RCV003049389] | Chr9:114300673 [GRCh38] Chr9:117062953 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4639-15C>T | single nucleotide variant | not provided [RCV003064196] | Chr9:114300610 [GRCh38] Chr9:117062890 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2809G>A (p.Gly937Arg) | single nucleotide variant | not provided [RCV002598794] | Chr9:114240461 [GRCh38] Chr9:117002741 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1909-3C>T | single nucleotide variant | not provided [RCV003090121] | Chr9:114178288 [GRCh38] Chr9:116940568 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3186G>A (p.Lys1062=) | single nucleotide variant | not provided [RCV002646741] | Chr9:114258585 [GRCh38] Chr9:117020865 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3234G>A (p.Gly1078=) | single nucleotide variant | not provided [RCV003010056] | Chr9:114264393 [GRCh38] Chr9:117026673 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2985T>C (p.Phe995=) | single nucleotide variant | not provided [RCV002745920] | Chr9:114250620 [GRCh38] Chr9:117012900 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2881-4G>T | single nucleotide variant | not provided [RCV002720375] | Chr9:114243503 [GRCh38] Chr9:117005783 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.424C>T (p.Arg142Trp) | single nucleotide variant | Inborn genetic diseases [RCV002812592] | Chr9:114167979 [GRCh38] Chr9:116930259 [GRCh37] Chr9:9q32 |
uncertain significance |
NC_000009.12:g.114258542_114258551del | deletion | not provided [RCV003031286] | Chr9:114258537..114258546 [GRCh38] Chr9:117020817..117020826 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4780C>T (p.Arg1594Cys) | single nucleotide variant | not provided [RCV002650287] | Chr9:114301308 [GRCh38] Chr9:117063588 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.723G>T (p.Thr241=) | single nucleotide variant | not provided [RCV003048901] | Chr9:114168278 [GRCh38] Chr9:116930558 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3834T>G (p.Pro1278=) | single nucleotide variant | not provided [RCV002811248] | Chr9:114282519 [GRCh38] Chr9:117044799 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2180G>A (p.Gly727Glu) | single nucleotide variant | not provided [RCV002649799] | Chr9:114205769 [GRCh38] Chr9:116968049 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3392C>T (p.Pro1131Leu) | single nucleotide variant | not provided [RCV003065775] | Chr9:114265474 [GRCh38] Chr9:117027754 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1963-2A>G | single nucleotide variant | not provided [RCV003026406] | Chr9:114183020 [GRCh38] Chr9:116945300 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.1247C>G (p.Ala416Gly) | single nucleotide variant | Inborn genetic diseases [RCV002809221] | Chr9:114168802 [GRCh38] Chr9:116931082 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4114C>T (p.Gln1372Ter) | single nucleotide variant | not provided [RCV002899125] | Chr9:114288929 [GRCh38] Chr9:117051209 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4638+14C>T | single nucleotide variant | not provided [RCV003061069] | Chr9:114300137 [GRCh38] Chr9:117062417 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2545C>T (p.Pro849Ser) | single nucleotide variant | Inborn genetic diseases [RCV002878587] | Chr9:114231846 [GRCh38] Chr9:116994126 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1909-13G>T | single nucleotide variant | not provided [RCV003060330] | Chr9:114178278 [GRCh38] Chr9:116940558 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.775A>G (p.Thr259Ala) | single nucleotide variant | not provided [RCV002770206] | Chr9:114168330 [GRCh38] Chr9:116930610 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4251G>A (p.Arg1417=) | single nucleotide variant | not provided [RCV002857353] | Chr9:114290102 [GRCh38] Chr9:117052382 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2226G>A (p.Gly742=) | single nucleotide variant | not provided [RCV003088372] | Chr9:114206254 [GRCh38] Chr9:116968534 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1865del (p.Leu622fs) | deletion | not provided [RCV002877286] | Chr9:114169420 [GRCh38] Chr9:116931700 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2715C>G (p.Pro905=) | single nucleotide variant | not provided [RCV003062710] | Chr9:114237703 [GRCh38] Chr9:116999983 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4206+10_4206+11insG | insertion | not provided [RCV002598934] | Chr9:114289305..114289306 [GRCh38] Chr9:117051585..117051586 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5531C>T (p.Ala1844Val) | single nucleotide variant | not provided [RCV002646188] | Chr9:114310643 [GRCh38] Chr9:117072923 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5073G>T (p.Arg1691Ser) | single nucleotide variant | Inborn genetic diseases [RCV002629247]|not provided [RCV002629246] | Chr9:114306654 [GRCh38] Chr9:117068934 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4550G>C (p.Gly1517Ala) | single nucleotide variant | not provided [RCV003044680] | Chr9:114292176 [GRCh38] Chr9:117054456 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.417C>A (p.Leu139=) | single nucleotide variant | not provided [RCV002857679] | Chr9:114167972 [GRCh38] Chr9:116930252 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4822C>T (p.Pro1608Ser) | single nucleotide variant | not provided [RCV002646289] | Chr9:114301694 [GRCh38] Chr9:117063974 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3243C>T (p.Gly1081=) | single nucleotide variant | not provided [RCV003046054] | Chr9:114264402 [GRCh38] Chr9:117026682 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1431C>T (p.Ser477=) | single nucleotide variant | not provided [RCV002898748] | Chr9:114168986 [GRCh38] Chr9:116931266 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3447+2T>C | single nucleotide variant | not provided [RCV003010009] | Chr9:114266620 [GRCh38] Chr9:117028900 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3423G>T (p.Gly1141=) | single nucleotide variant | not provided [RCV002856987] | Chr9:114266594 [GRCh38] Chr9:117028874 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4503G>A (p.Leu1501=) | single nucleotide variant | not provided [RCV002806945] | Chr9:114292129 [GRCh38] Chr9:117054409 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3135A>G (p.Gly1045=) | single nucleotide variant | not provided [RCV002791674] | Chr9:114252926 [GRCh38] Chr9:117015206 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3840T>C (p.Thr1280=) | single nucleotide variant | not provided [RCV002806460] | Chr9:114282525 [GRCh38] Chr9:117044805 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1805C>T (p.Pro602Leu) | single nucleotide variant | not provided [RCV002937601] | Chr9:114169360 [GRCh38] Chr9:116931640 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3757C>T (p.Arg1253Cys) | single nucleotide variant | not provided [RCV003062920] | Chr9:114282316 [GRCh38] Chr9:117044596 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2211C>T (p.Tyr737=) | single nucleotide variant | not provided [RCV002856425] | Chr9:114205800 [GRCh38] Chr9:116968080 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4920T>C (p.Ser1640=) | single nucleotide variant | not provided [RCV002715602] | Chr9:114304655 [GRCh38] Chr9:117066935 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4477-5T>C | single nucleotide variant | not provided [RCV003088520] | Chr9:114292098 [GRCh38] Chr9:117054378 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4098+15T>C | single nucleotide variant | not provided [RCV003063468] | Chr9:114288770 [GRCh38] Chr9:117051050 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2466+11_2466+12insA | insertion | not provided [RCV002600874] | Chr9:114222278..114222279 [GRCh38] Chr9:116984558..116984559 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3556-9C>T | single nucleotide variant | not provided [RCV003029856] | Chr9:114270719 [GRCh38] Chr9:117032999 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2547C>G (p.Pro849=) | single nucleotide variant | not provided [RCV002597540] | Chr9:114231848 [GRCh38] Chr9:116994128 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1708G>T (p.Asp570Tyr) | single nucleotide variant | not provided [RCV003061148] | Chr9:114169263 [GRCh38] Chr9:116931543 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.116C>T (p.Thr39Ile) | single nucleotide variant | not provided [RCV003063527] | Chr9:114162768 [GRCh38] Chr9:116925048 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.63-4C>T | single nucleotide variant | not provided [RCV003030972] | Chr9:114162711 [GRCh38] Chr9:116924991 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3612G>A (p.Gly1204=) | single nucleotide variant | not provided [RCV003029630] | Chr9:114275663 [GRCh38] Chr9:117037943 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3934-15_3934-13del | microsatellite | not provided [RCV002720056] | Chr9:114284706..114284708 [GRCh38] Chr9:117046986..117046988 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.62+8C>G | single nucleotide variant | not provided [RCV003010315] | Chr9:114156020 [GRCh38] Chr9:116918300 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2446_2447delinsA (p.Pro816fs) | indel | not provided [RCV003011313] | Chr9:114222247..114222248 [GRCh38] Chr9:116984527..116984528 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.5070C>T (p.Cys1690=) | single nucleotide variant | not provided [RCV003011323] | Chr9:114306651 [GRCh38] Chr9:117068931 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4785G>A (p.Gly1595=) | single nucleotide variant | not provided [RCV002899414] | Chr9:114301313 [GRCh38] Chr9:117063593 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1234C>T (p.Arg412Cys) | single nucleotide variant | not provided [RCV003060715] | Chr9:114168789 [GRCh38] Chr9:116931069 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1959T>C (p.Pro653=) | single nucleotide variant | not provided [RCV003086285] | Chr9:114178341 [GRCh38] Chr9:116940621 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1218A>C (p.Gln406His) | single nucleotide variant | not provided [RCV002630496] | Chr9:114168773 [GRCh38] Chr9:116931053 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2268+7G>T | single nucleotide variant | not provided [RCV002627634] | Chr9:114206303 [GRCh38] Chr9:116968583 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1602G>A (p.Lys534=) | single nucleotide variant | not provided [RCV003044727] | Chr9:114169157 [GRCh38] Chr9:116931437 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1410G>A (p.Lys470=) | single nucleotide variant | not provided [RCV002899031] | Chr9:114168965 [GRCh38] Chr9:116931245 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2238G>T (p.Pro746=) | single nucleotide variant | not provided [RCV002581035] | Chr9:114206266 [GRCh38] Chr9:116968546 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4098+7A>G | single nucleotide variant | not provided [RCV002961890] | Chr9:114288762 [GRCh38] Chr9:117051042 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.15G>A (p.Ser5=) | single nucleotide variant | not provided [RCV002833401] | Chr9:114155965 [GRCh38] Chr9:116918245 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1908+17T>C | single nucleotide variant | not provided [RCV002581826] | Chr9:114169480 [GRCh38] Chr9:116931760 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5545C>A (p.Gln1849Lys) | single nucleotide variant | not provided [RCV002922368] | Chr9:114310657 [GRCh38] Chr9:117072937 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4272G>A (p.Gly1424=) | single nucleotide variant | not provided [RCV002630258] | Chr9:114290235 [GRCh38] Chr9:117052515 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.242G>A (p.Arg81Gln) | single nucleotide variant | Inborn genetic diseases [RCV002939672] | Chr9:114167797 [GRCh38] Chr9:116930077 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.614A>T (p.His205Leu) | single nucleotide variant | not provided [RCV002806647] | Chr9:114168169 [GRCh38] Chr9:116930449 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2653C>T (p.Arg885Trp) | single nucleotide variant | Inborn genetic diseases [RCV003062540]|not provided [RCV003062539] | Chr9:114237014 [GRCh38] Chr9:116999294 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5292C>T (p.Thr1764=) | single nucleotide variant | not provided [RCV002835106] | Chr9:114309334 [GRCh38] Chr9:117071614 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2589G>C (p.Val863=) | single nucleotide variant | not provided [RCV003030418] | Chr9:114235622 [GRCh38] Chr9:116997902 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4368+17_4368+32del | deletion | not provided [RCV002811362] | Chr9:114290344..114290359 [GRCh38] Chr9:117052624..117052639 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1113G>C (p.Lys371Asn) | single nucleotide variant | not provided [RCV002834750] | Chr9:114168668 [GRCh38] Chr9:116930948 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3195+7C>G | single nucleotide variant | not provided [RCV003064027] | Chr9:114258601 [GRCh38] Chr9:117020881 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3378C>T (p.Gly1126=) | single nucleotide variant | not provided [RCV003009712] | Chr9:114265460 [GRCh38] Chr9:117027740 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5359C>A (p.Arg1787Ser) | single nucleotide variant | Inborn genetic diseases [RCV002835923] | Chr9:114309401 [GRCh38] Chr9:117071681 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5108-11G>A | single nucleotide variant | not provided [RCV003087870] | Chr9:114307658 [GRCh38] Chr9:117069938 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3609+9C>T | single nucleotide variant | not provided [RCV002770832] | Chr9:114270790 [GRCh38] Chr9:117033070 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4501C>T (p.Leu1501=) | single nucleotide variant | not provided [RCV003063264] | Chr9:114292127 [GRCh38] Chr9:117054407 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2835+9G>A | single nucleotide variant | not provided [RCV002576950] | Chr9:114240496 [GRCh38] Chr9:117002776 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2673+8C>T | single nucleotide variant | not provided [RCV003044266] | Chr9:114237042 [GRCh38] Chr9:116999322 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4840C>A (p.Pro1614Thr) | single nucleotide variant | not provided [RCV003089380] | Chr9:114301712 [GRCh38] Chr9:117063992 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2501C>T (p.Pro834Leu) | single nucleotide variant | not provided [RCV002922288] | Chr9:114231113 [GRCh38] Chr9:116993393 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3250-19C>T | single nucleotide variant | not provided [RCV002629641] | Chr9:114264905 [GRCh38] Chr9:117027185 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1869G>T (p.Leu623=) | single nucleotide variant | not provided [RCV002680850] | Chr9:114169424 [GRCh38] Chr9:116931704 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2914C>T (p.Pro972Ser) | single nucleotide variant | not provided [RCV002634181] | Chr9:114243540 [GRCh38] Chr9:117005820 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2170-13T>G | single nucleotide variant | not provided [RCV003068850] | Chr9:114205746 [GRCh38] Chr9:116968026 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.42G>A (p.Ala14=) | single nucleotide variant | not provided [RCV003069893] | Chr9:114155992 [GRCh38] Chr9:116918272 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4924G>A (p.Ala1642Thr) | single nucleotide variant | not provided [RCV002634064] | Chr9:114304659 [GRCh38] Chr9:117066939 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2848C>A (p.Pro950Thr) | single nucleotide variant | not provided [RCV003092778] | Chr9:114242199 [GRCh38] Chr9:117004479 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.195G>A (p.Pro65=) | single nucleotide variant | not provided [RCV002942995] | Chr9:114167750 [GRCh38] Chr9:116930030 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2957G>C (p.Arg986Pro) | single nucleotide variant | not provided [RCV002653655] | Chr9:114245888 [GRCh38] Chr9:117008168 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2521-7C>T | single nucleotide variant | not provided [RCV002654303] | Chr9:114231815 [GRCh38] Chr9:116994095 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2979+14G>A | single nucleotide variant | not provided [RCV003066591] | Chr9:114245924 [GRCh38] Chr9:117008204 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3478C>T (p.Leu1160Phe) | single nucleotide variant | not provided [RCV002633768] | Chr9:114267534 [GRCh38] Chr9:117029814 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1780C>T (p.Pro594Ser) | single nucleotide variant | not provided [RCV003068904] | Chr9:114169335 [GRCh38] Chr9:116931615 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1009C>T (p.Leu337Phe) | single nucleotide variant | not provided [RCV003066151] | Chr9:114168564 [GRCh38] Chr9:116930844 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1235G>C (p.Arg412Pro) | single nucleotide variant | not provided [RCV003052490] | Chr9:114168790 [GRCh38] Chr9:116931070 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3685C>T (p.Pro1229Ser) | single nucleotide variant | not provided [RCV003051500] | Chr9:114275736 [GRCh38] Chr9:117038016 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.409G>A (p.Val137Ile) | single nucleotide variant | not provided [RCV002654972] | Chr9:114167964 [GRCh38] Chr9:116930244 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1771G>A (p.Val591Ile) | single nucleotide variant | not provided [RCV002653393] | Chr9:114169326 [GRCh38] Chr9:116931606 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3772-12C>T | single nucleotide variant | not provided [RCV003071414] | Chr9:114282445 [GRCh38] Chr9:117044725 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2979+13C>T | single nucleotide variant | not provided [RCV003050989] | Chr9:114245923 [GRCh38] Chr9:117008203 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4317C>T (p.Gly1439=) | single nucleotide variant | not provided [RCV003051025] | Chr9:114290280 [GRCh38] Chr9:117052560 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1881G>A (p.Pro627=) | single nucleotide variant | not provided [RCV002654879] | Chr9:114169436 [GRCh38] Chr9:116931716 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4308C>T (p.Gly1436=) | single nucleotide variant | not provided [RCV003051882] | Chr9:114290271 [GRCh38] Chr9:117052551 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1763C>T (p.Pro588Leu) | single nucleotide variant | not provided [RCV003073036] | Chr9:114169318 [GRCh38] Chr9:116931598 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1258C>G (p.Arg420Gly) | single nucleotide variant | not provided [RCV003072063] | Chr9:114168813 [GRCh38] Chr9:116931093 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4587C>T (p.Gly1529=) | single nucleotide variant | not provided [RCV003093508] | Chr9:114300072 [GRCh38] Chr9:117062352 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3141+18G>T | single nucleotide variant | not provided [RCV003068117] | Chr9:114252950 [GRCh38] Chr9:117015230 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4006G>A (p.Gly1336Ser) | single nucleotide variant | not provided [RCV003092937] | Chr9:114288473 [GRCh38] Chr9:117050753 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2956C>T (p.Arg986Trp) | single nucleotide variant | Inborn genetic diseases [RCV003269399]|not provided [RCV003050787] | Chr9:114245887 [GRCh38] Chr9:117008167 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2819G>A (p.Gly940Glu) | single nucleotide variant | not provided [RCV002585596] | Chr9:114240471 [GRCh38] Chr9:117002751 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5356G>A (p.Val1786Ile) | single nucleotide variant | not provided [RCV003069973] | Chr9:114309398 [GRCh38] Chr9:117071678 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2979+4A>G | single nucleotide variant | not provided [RCV003072382] | Chr9:114245914 [GRCh38] Chr9:117008194 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.532C>T (p.Arg178Trp) | single nucleotide variant | not provided [RCV002610844] | Chr9:114168087 [GRCh38] Chr9:116930367 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2830C>T (p.Pro944Ser) | single nucleotide variant | not provided [RCV002613024] | Chr9:114240482 [GRCh38] Chr9:117002762 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5359C>T (p.Arg1787Cys) | single nucleotide variant | not provided [RCV002588578] | Chr9:114309401 [GRCh38] Chr9:117071681 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1999G>A (p.Gly667Ser) | single nucleotide variant | not provided [RCV003051182] | Chr9:114183058 [GRCh38] Chr9:116945338 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.153G>T (p.Arg51=) | single nucleotide variant | not provided [RCV002585148] | Chr9:114167708 [GRCh38] Chr9:116929988 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4813C>T (p.Pro1605Ser) | single nucleotide variant | not provided [RCV003071668] | Chr9:114301685 [GRCh38] Chr9:117063965 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3693C>G (p.Gly1231=) | single nucleotide variant | not provided [RCV002654289] | Chr9:114275744 [GRCh38] Chr9:117038024 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2296G>A (p.Gly766Ser) | single nucleotide variant | not provided [RCV002611396] | Chr9:114209702 [GRCh38] Chr9:116971982 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1226C>T (p.Pro409Leu) | single nucleotide variant | not provided [RCV003071892] | Chr9:114168781 [GRCh38] Chr9:116931061 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3501+13G>A | single nucleotide variant | not provided [RCV003666117] | Chr9:114267570 [GRCh38] Chr9:117029850 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2639G>C (p.Gly880Ala) | single nucleotide variant | not provided [RCV002611581] | Chr9:114237000 [GRCh38] Chr9:116999280 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.5218-8C>G | single nucleotide variant | not provided [RCV002611747] | Chr9:114309252 [GRCh38] Chr9:117071532 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4169G>C (p.Arg1390Pro) | single nucleotide variant | not provided [RCV003072504] | Chr9:114289258 [GRCh38] Chr9:117051538 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4123C>T (p.Arg1375Cys) | single nucleotide variant | not provided [RCV003068559] | Chr9:114288938 [GRCh38] Chr9:117051218 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3316C>T (p.His1106Tyr) | single nucleotide variant | not provided [RCV003068566] | Chr9:114265087 [GRCh38] Chr9:117027367 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3393G>A (p.Pro1131=) | single nucleotide variant | not provided [RCV002612225] | Chr9:114265475 [GRCh38] Chr9:117027755 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4276C>T (p.Pro1426Ser) | single nucleotide variant | not provided [RCV003070520] | Chr9:114290239 [GRCh38] Chr9:117052519 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.860G>A (p.Gly287Glu) | single nucleotide variant | not provided [RCV002589898] | Chr9:114168415 [GRCh38] Chr9:116930695 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1061A>G (p.Gln354Arg) | single nucleotide variant | not provided [RCV002721372] | Chr9:114168616 [GRCh38] Chr9:116930896 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1753C>G (p.Gln585Glu) | single nucleotide variant | not provided [RCV002653880] | Chr9:114169308 [GRCh38] Chr9:116931588 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3645T>C (p.His1215=) | single nucleotide variant | not provided [RCV003068933] | Chr9:114275696 [GRCh38] Chr9:117037976 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2335G>A (p.Val779Ile) | single nucleotide variant | not provided [RCV002606970] | Chr9:114210994 [GRCh38] Chr9:116973274 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3361C>T (p.Pro1121Ser) | single nucleotide variant | not provided [RCV003073249] | Chr9:114265443 [GRCh38] Chr9:117027723 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4291G>A (p.Val1431Met) | single nucleotide variant | not provided [RCV002612648] | Chr9:114290254 [GRCh38] Chr9:117052534 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1322G>A (p.Arg441Gln) | single nucleotide variant | not provided [RCV003071123] | Chr9:114168877 [GRCh38] Chr9:116931157 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2443C>T (p.Pro815Ser) | single nucleotide variant | Inborn genetic diseases [RCV003214291] | Chr9:114222244 [GRCh38] Chr9:116984524 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4736T>C (p.Leu1579Pro) | single nucleotide variant | Inborn genetic diseases [RCV003194142] | Chr9:114301106 [GRCh38] Chr9:117063386 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2417A>T (p.Asn806Ile) | single nucleotide variant | Inborn genetic diseases [RCV003194644] | Chr9:114219840 [GRCh38] Chr9:116982120 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3463G>T (p.Val1155Leu) | single nucleotide variant | Inborn genetic diseases [RCV003215970] | Chr9:114267519 [GRCh38] Chr9:117029799 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1901G>C (p.Gly634Ala) | single nucleotide variant | Inborn genetic diseases [RCV003201429] | Chr9:114169456 [GRCh38] Chr9:116931736 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4357dup (p.Ala1453fs) | duplication | Steel syndrome [RCV003143606]|not provided [RCV003730408] | Chr9:114290319..114290320 [GRCh38] Chr9:117052599..117052600 [GRCh37] Chr9:9q32 |
pathogenic|likely pathogenic |
NM_032888.4(COL27A1):c.358C>T (p.Gln120Ter) | single nucleotide variant | Steel syndrome [RCV003143598] | Chr9:114167913 [GRCh38] Chr9:116930193 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3754G>T (p.Gly1252Cys) | single nucleotide variant | Steel syndrome [RCV003141678] | Chr9:114282313 [GRCh38] Chr9:117044593 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4441G>A (p.Gly1481Ser) | single nucleotide variant | Steel syndrome [RCV003141679] | Chr9:114290882 [GRCh38] Chr9:117053162 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4781G>A (p.Arg1594His) | single nucleotide variant | Inborn genetic diseases [RCV003212635] | Chr9:114301309 [GRCh38] Chr9:117063589 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1695T>A (p.Asp565Glu) | single nucleotide variant | Inborn genetic diseases [RCV003217838] | Chr9:114169250 [GRCh38] Chr9:116931530 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1289C>A (p.Pro430Gln) | single nucleotide variant | Inborn genetic diseases [RCV003212904] | Chr9:114168844 [GRCh38] Chr9:116931124 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4681C>T (p.Arg1561Trp) | single nucleotide variant | Inborn genetic diseases [RCV003209051] | Chr9:114300667 [GRCh38] Chr9:117062947 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1190C>A (p.Thr397Lys) | single nucleotide variant | Inborn genetic diseases [RCV003181271] | Chr9:114168745 [GRCh38] Chr9:116931025 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2544G>C (p.Glu848Asp) | single nucleotide variant | Inborn genetic diseases [RCV003193844] | Chr9:114231845 [GRCh38] Chr9:116994125 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4G>A (p.Gly2Arg) | single nucleotide variant | Inborn genetic diseases [RCV003197513] | Chr9:114155954 [GRCh38] Chr9:116918234 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1636G>A (p.Gly546Arg) | single nucleotide variant | Inborn genetic diseases [RCV003307137] | Chr9:114169191 [GRCh38] Chr9:116931471 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2088T>A (p.Pro696=) | single nucleotide variant | not provided [RCV003568945] | Chr9:114195976 [GRCh38] Chr9:116958256 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4765G>C (p.Gly1589Arg) | single nucleotide variant | not specified [RCV003324248] | Chr9:114301293 [GRCh38] Chr9:117063573 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2855G>A (p.Gly952Glu) | single nucleotide variant | not specified [RCV003331816] | Chr9:114242206 [GRCh38] Chr9:117004486 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3178G>C (p.Gly1060Arg) | single nucleotide variant | not specified [RCV003331824] | Chr9:114258577 [GRCh38] Chr9:117020857 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1324C>G (p.Pro442Ala) | single nucleotide variant | Inborn genetic diseases [RCV003381005] | Chr9:114168879 [GRCh38] Chr9:116931159 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3394G>A (p.Gly1132Ser) | single nucleotide variant | not specified [RCV003332019] | Chr9:114266565 [GRCh38] Chr9:117028845 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1892G>A (p.Gly631Glu) | single nucleotide variant | not specified [RCV003331820] | Chr9:114169447 [GRCh38] Chr9:116931727 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2833G>A (p.Glu945Lys) | single nucleotide variant | Inborn genetic diseases [RCV003349549] | Chr9:114240485 [GRCh38] Chr9:117002765 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1376G>A (p.Arg459Gln) | single nucleotide variant | Inborn genetic diseases [RCV003349190] | Chr9:114168931 [GRCh38] Chr9:116931211 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4793G>T (p.Gly1598Val) | single nucleotide variant | Inborn genetic diseases [RCV003373706] | Chr9:114301446 [GRCh38] Chr9:117063726 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3136C>T (p.Pro1046Ser) | single nucleotide variant | Inborn genetic diseases [RCV003353676] | Chr9:114252927 [GRCh38] Chr9:117015207 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1447C>A (p.Pro483Thr) | single nucleotide variant | Inborn genetic diseases [RCV003370074] | Chr9:114169002 [GRCh38] Chr9:116931282 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.881C>T (p.Pro294Leu) | single nucleotide variant | Inborn genetic diseases [RCV003385945] | Chr9:114168436 [GRCh38] Chr9:116930716 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2119C>A (p.Arg707=) | single nucleotide variant | not provided [RCV003569883] | Chr9:114196007 [GRCh38] Chr9:116958287 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5218-12G>C | single nucleotide variant | not provided [RCV003875222] | Chr9:114309248 [GRCh38] Chr9:117071528 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5298C>T (p.His1766=) | single nucleotide variant | not provided [RCV003570820] | Chr9:114309340 [GRCh38] Chr9:117071620 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2367+17T>C | single nucleotide variant | not provided [RCV003712611] | Chr9:114211043 [GRCh38] Chr9:116973323 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2649T>G (p.Gly883=) | single nucleotide variant | not provided [RCV003543517] | Chr9:114237010 [GRCh38] Chr9:116999290 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3394-18TGTC[2] | microsatellite | not provided [RCV003875611] | Chr9:114266547..114266550 [GRCh38] Chr9:117028827..117028830 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4746G>C (p.Ser1582=) | single nucleotide variant | not provided [RCV003570563] | Chr9:114301116 [GRCh38] Chr9:117063396 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4872+13C>T | single nucleotide variant | not provided [RCV003570914] | Chr9:114302121 [GRCh38] Chr9:117064401 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5166C>T (p.Cys1722=) | single nucleotide variant | not provided [RCV003570978] | Chr9:114307727 [GRCh38] Chr9:117070007 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2412T>C (p.Asp804=) | single nucleotide variant | not provided [RCV003875478] | Chr9:114219835 [GRCh38] Chr9:116982115 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2566-12G>A | single nucleotide variant | not provided [RCV003875026] | Chr9:114235587 [GRCh38] Chr9:116997867 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4584+2T>C | single nucleotide variant | not provided [RCV003570551] | Chr9:114292212 [GRCh38] Chr9:117054492 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4585-4G>T | single nucleotide variant | not provided [RCV003571080] | Chr9:114300066 [GRCh38] Chr9:117062346 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4643C>G (p.Pro1548Arg) | single nucleotide variant | Steel syndrome [RCV003479546] | Chr9:114300629 [GRCh38] Chr9:117062909 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2017-17A>G | single nucleotide variant | not provided [RCV003542966] | Chr9:114194387 [GRCh38] Chr9:116956667 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3196-4C>A | single nucleotide variant | not provided [RCV003571067] | Chr9:114264351 [GRCh38] Chr9:117026631 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2224-16G>A | single nucleotide variant | not provided [RCV003872913] | Chr9:114206236 [GRCh38] Chr9:116968516 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4809+1G>A | single nucleotide variant | not provided [RCV003543234] | Chr9:114301463 [GRCh38] Chr9:117063743 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3934-19C>T | single nucleotide variant | not provided [RCV003825359] | Chr9:114284705 [GRCh38] Chr9:117046985 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.969A>G (p.Leu323=) | single nucleotide variant | not provided [RCV003569554] | Chr9:114168524 [GRCh38] Chr9:116930804 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2116G>A (p.Gly706Arg) | single nucleotide variant | COL27A1-related condition [RCV003405962] | Chr9:114196004 [GRCh38] Chr9:116958284 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4152+15G>A | single nucleotide variant | not provided [RCV003852870] | Chr9:114288982 [GRCh38] Chr9:117051262 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3339+14del | deletion | not provided [RCV003690604] | Chr9:114265124 [GRCh38] Chr9:117027404 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1579G>A (p.Gly527Ser) | single nucleotide variant | not provided [RCV003443841] | Chr9:114169134 [GRCh38] Chr9:116931414 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.420G>A (p.Gly140=) | single nucleotide variant | not provided [RCV003430212] | Chr9:114167975 [GRCh38] Chr9:116930255 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1491T>A (p.Ser497=) | single nucleotide variant | not provided [RCV003425761] | Chr9:114169046 [GRCh38] Chr9:116931326 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.257C>T (p.Thr86Met) | single nucleotide variant | not provided [RCV003430211] | Chr9:114167812 [GRCh38] Chr9:116930092 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3295-15C>T | single nucleotide variant | not provided [RCV003696352] | Chr9:114265051 [GRCh38] Chr9:117027331 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4846-14dup | duplication | not provided [RCV003738682] | Chr9:114302067..114302068 [GRCh38] Chr9:117064347..117064348 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4369-13G>T | single nucleotide variant | not provided [RCV003696474] | Chr9:114290797 [GRCh38] Chr9:117053077 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4702-19G>A | single nucleotide variant | not provided [RCV003695245] | Chr9:114301053 [GRCh38] Chr9:117063333 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2394A>G (p.Arg798=) | single nucleotide variant | not provided [RCV003687112] | Chr9:114219817 [GRCh38] Chr9:116982097 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3295-15C>G | single nucleotide variant | not provided [RCV003828333] | Chr9:114265051 [GRCh38] Chr9:117027331 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3718-13C>T | single nucleotide variant | not provided [RCV003740263] | Chr9:114282264 [GRCh38] Chr9:117044544 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4152+20C>G | single nucleotide variant | not provided [RCV003881756] | Chr9:114288987 [GRCh38] Chr9:117051267 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3294+7C>T | single nucleotide variant | not provided [RCV003579061] | Chr9:114264975 [GRCh38] Chr9:117027255 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2124+7T>C | single nucleotide variant | not provided [RCV003694636] | Chr9:114196019 [GRCh38] Chr9:116958299 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3988-5C>G | single nucleotide variant | not provided [RCV003579443] | Chr9:114288450 [GRCh38] Chr9:117050730 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5349G>A (p.Lys1783=) | single nucleotide variant | not provided [RCV003824905] | Chr9:114309391 [GRCh38] Chr9:117071671 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2727+18T>G | single nucleotide variant | not provided [RCV003695794] | Chr9:114237733 [GRCh38] Chr9:117000013 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3933+16C>T | single nucleotide variant | not provided [RCV003693917] | Chr9:114283778 [GRCh38] Chr9:117046058 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.663G>A (p.Val221=) | single nucleotide variant | not provided [RCV003686370] | Chr9:114168218 [GRCh38] Chr9:116930498 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1665C>A (p.Val555=) | single nucleotide variant | not provided [RCV003738703] | Chr9:114169220 [GRCh38] Chr9:116931500 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3934-13T>C | single nucleotide variant | not provided [RCV003738710] | Chr9:114284711 [GRCh38] Chr9:117046991 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3774T>A (p.Gly1258=) | single nucleotide variant | not provided [RCV003689347] | Chr9:114282459 [GRCh38] Chr9:117044739 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3933+12T>C | single nucleotide variant | not provided [RCV003738793] | Chr9:114283774 [GRCh38] Chr9:117046054 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4585-7C>G | single nucleotide variant | not provided [RCV003579178] | Chr9:114300063 [GRCh38] Chr9:117062343 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3195+2T>G | single nucleotide variant | not provided [RCV003578122] | Chr9:114258596 [GRCh38] Chr9:117020876 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.1323G>T (p.Arg441=) | single nucleotide variant | not provided [RCV003577562] | Chr9:114168878 [GRCh38] Chr9:116931158 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3783C>T (p.Gly1261=) | single nucleotide variant | not provided [RCV003695416] | Chr9:114282468 [GRCh38] Chr9:117044748 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3610-16A>T | single nucleotide variant | not provided [RCV003578149] | Chr9:114275645 [GRCh38] Chr9:117037925 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4671C>A (p.Ile1557=) | single nucleotide variant | not provided [RCV003689539] | Chr9:114300657 [GRCh38] Chr9:117062937 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4099-18T>C | single nucleotide variant | not provided [RCV003826600] | Chr9:114288896 [GRCh38] Chr9:117051176 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4585-13G>C | single nucleotide variant | not provided [RCV003661869] | Chr9:114300057 [GRCh38] Chr9:117062337 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4207-18T>C | single nucleotide variant | not provided [RCV003574210] | Chr9:114290040 [GRCh38] Chr9:117052320 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4722G>T (p.Gly1574=) | single nucleotide variant | not provided [RCV003690609] | Chr9:114301092 [GRCh38] Chr9:117063372 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5217+1G>A | single nucleotide variant | not provided [RCV003544193] | Chr9:114307779 [GRCh38] Chr9:117070059 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4791+11G>C | single nucleotide variant | not provided [RCV003546995] | Chr9:114301330 [GRCh38] Chr9:117063610 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5217+18C>A | single nucleotide variant | not provided [RCV003693802] | Chr9:114307796 [GRCh38] Chr9:117070076 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-19C>A | single nucleotide variant | not provided [RCV003739022] | Chr9:114290205 [GRCh38] Chr9:117052485 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3144T>C (p.Gly1048=) | single nucleotide variant | not provided [RCV003694901] | Chr9:114258543 [GRCh38] Chr9:117020823 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4639-9C>T | single nucleotide variant | not provided [RCV003825894] | Chr9:114300616 [GRCh38] Chr9:117062896 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3312A>G (p.Arg1104=) | single nucleotide variant | not provided [RCV003576875] | Chr9:114265083 [GRCh38] Chr9:117027363 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4260+15C>G | single nucleotide variant | not provided [RCV003829061] | Chr9:114290126 [GRCh38] Chr9:117052406 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1201C>T (p.Leu401=) | single nucleotide variant | not provided [RCV003544418] | Chr9:114168756 [GRCh38] Chr9:116931036 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.51G>A (p.Ala17=) | single nucleotide variant | not provided [RCV003573059] | Chr9:114156001 [GRCh38] Chr9:116918281 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1908+15G>A | single nucleotide variant | not provided [RCV003575794] | Chr9:114169478 [GRCh38] Chr9:116931758 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3717+16C>T | single nucleotide variant | not provided [RCV003881992] | Chr9:114275784 [GRCh38] Chr9:117038064 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4938+19C>T | single nucleotide variant | not provided [RCV003572438] | Chr9:114304692 [GRCh38] Chr9:117066972 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5107+19G>C | single nucleotide variant | not provided [RCV003713856] | Chr9:114306707 [GRCh38] Chr9:117068987 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1989A>C (p.Pro663=) | single nucleotide variant | not provided [RCV003827668] | Chr9:114183048 [GRCh38] Chr9:116945328 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2781+9C>T | single nucleotide variant | not provided [RCV003662180] | Chr9:114240282 [GRCh38] Chr9:117002562 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3087+19T>C | single nucleotide variant | not provided [RCV003880461] | Chr9:114252665 [GRCh38] Chr9:117014945 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2620-17C>T | single nucleotide variant | not provided [RCV003713947] | Chr9:114236964 [GRCh38] Chr9:116999244 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.513G>T (p.Val171=) | single nucleotide variant | not provided [RCV003573204] | Chr9:114168068 [GRCh38] Chr9:116930348 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4701+8C>A | single nucleotide variant | not provided [RCV003713980] | Chr9:114300695 [GRCh38] Chr9:117062975 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2223+11T>C | single nucleotide variant | not provided [RCV003882100] | Chr9:114205823 [GRCh38] Chr9:116968103 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1653C>A (p.Pro551=) | single nucleotide variant | not provided [RCV003882252] | Chr9:114169208 [GRCh38] Chr9:116931488 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5376T>C (p.Asn1792=) | single nucleotide variant | not provided [RCV003576181] | Chr9:114309418 [GRCh38] Chr9:117071698 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.99del (p.Cys34fs) | deletion | not provided [RCV003578440] | Chr9:114162750 [GRCh38] Chr9:116925030 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2553G>T (p.Leu851=) | single nucleotide variant | not provided [RCV003574030] | Chr9:114231854 [GRCh38] Chr9:116994134 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4515C>A (p.Gly1505=) | single nucleotide variant | not provided [RCV003661586] | Chr9:114292141 [GRCh38] Chr9:117054421 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5062C>A (p.Arg1688=) | single nucleotide variant | not provided [RCV003695675] | Chr9:114306643 [GRCh38] Chr9:117068923 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3987+11G>A | single nucleotide variant | not provided [RCV003875719] | Chr9:114284788 [GRCh38] Chr9:117047068 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2125-2del | deletion | not provided [RCV003574125] | Chr9:114205100 [GRCh38] Chr9:116967380 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.3141+10G>A | single nucleotide variant | not provided [RCV003690025] | Chr9:114252942 [GRCh38] Chr9:117015222 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2565+15C>T | single nucleotide variant | not provided [RCV003739196] | Chr9:114231881 [GRCh38] Chr9:116994161 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3576T>G (p.Gly1192=) | single nucleotide variant | not provided [RCV003544745] | Chr9:114270748 [GRCh38] Chr9:117033028 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2782-13C>T | single nucleotide variant | not provided [RCV003573429] | Chr9:114240421 [GRCh38] Chr9:117002701 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2422-8A>C | single nucleotide variant | not provided [RCV003714875] | Chr9:114222215 [GRCh38] Chr9:116984495 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2125-8T>G | single nucleotide variant | not provided [RCV003662418] | Chr9:114205094 [GRCh38] Chr9:116967374 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3863del (p.Gly1288fs) | deletion | not provided [RCV003716204] | Chr9:114282545 [GRCh38] Chr9:117044825 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3933+23del | deletion | not provided [RCV003881634] | Chr9:114283782 [GRCh38] Chr9:117046062 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3447+17dup | duplication | not provided [RCV003576311] | Chr9:114266632..114266633 [GRCh38] Chr9:117028912..117028913 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2467-19del | deletion | not provided [RCV003881479] | Chr9:114231059 [GRCh38] Chr9:116993339 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.438C>T (p.Ala146=) | single nucleotide variant | not provided [RCV003714707] | Chr9:114167993 [GRCh38] Chr9:116930273 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2170-19T>C | single nucleotide variant | not provided [RCV003687702] | Chr9:114205740 [GRCh38] Chr9:116968020 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4299G>T (p.Gly1433=) | single nucleotide variant | not provided [RCV003578279] | Chr9:114290262 [GRCh38] Chr9:117052542 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2934+20C>T | single nucleotide variant | not provided [RCV003714710] | Chr9:114243580 [GRCh38] Chr9:117005860 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4206+16G>A | single nucleotide variant | not provided [RCV003739690] | Chr9:114289311 [GRCh38] Chr9:117051591 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3195+12C>A | single nucleotide variant | not provided [RCV003738643] | Chr9:114258606 [GRCh38] Chr9:117020886 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1788A>G (p.Gln596=) | single nucleotide variant | not provided [RCV003573412] | Chr9:114169343 [GRCh38] Chr9:116931623 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2637A>G (p.Pro879=) | single nucleotide variant | not provided [RCV003689996] | Chr9:114236998 [GRCh38] Chr9:116999278 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.734del (p.Pro245fs) | deletion | not provided [RCV003690496] | Chr9:114168286 [GRCh38] Chr9:116930566 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4477-13G>T | single nucleotide variant | not provided [RCV003661713] | Chr9:114292090 [GRCh38] Chr9:117054370 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4045-9G>T | single nucleotide variant | not provided [RCV003687987] | Chr9:114288693 [GRCh38] Chr9:117050973 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3234G>C (p.Gly1078=) | single nucleotide variant | not provided [RCV003546056] | Chr9:114264393 [GRCh38] Chr9:117026673 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4260+17G>A | single nucleotide variant | not provided [RCV003692684] | Chr9:114290128 [GRCh38] Chr9:117052408 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4972C>T (p.Gln1658Ter) | single nucleotide variant | not provided [RCV003693572] | Chr9:114306553 [GRCh38] Chr9:117068833 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.5108-15C>T | single nucleotide variant | not provided [RCV003686800] | Chr9:114307654 [GRCh38] Chr9:117069934 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3690dup (p.Gly1231fs) | duplication | not provided [RCV003572717] | Chr9:114275735..114275736 [GRCh38] Chr9:117038015..117038016 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3318C>T (p.His1106=) | single nucleotide variant | not provided [RCV003572849] | Chr9:114265089 [GRCh38] Chr9:117027369 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2881-15G>A | single nucleotide variant | not provided [RCV003687989] | Chr9:114243492 [GRCh38] Chr9:117005772 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1116T>C (p.Pro372=) | single nucleotide variant | not provided [RCV003715736] | Chr9:114168671 [GRCh38] Chr9:116930951 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1245T>C (p.Pro415=) | single nucleotide variant | not provided [RCV003576785] | Chr9:114168800 [GRCh38] Chr9:116931080 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-8T>C | single nucleotide variant | not provided [RCV003576796] | Chr9:114250607 [GRCh38] Chr9:117012887 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3717+11A>G | single nucleotide variant | not provided [RCV003739699] | Chr9:114275779 [GRCh38] Chr9:117038059 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.168G>A (p.Trp56Ter) | single nucleotide variant | not provided [RCV003691529] | Chr9:114167723 [GRCh38] Chr9:116930003 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.228T>C (p.Phe76=) | single nucleotide variant | not provided [RCV003691750] | Chr9:114167783 [GRCh38] Chr9:116930063 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.544C>T (p.Leu182=) | single nucleotide variant | not provided [RCV003691751] | Chr9:114168099 [GRCh38] Chr9:116930379 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4755+14T>C | single nucleotide variant | not provided [RCV003829082] | Chr9:114301139 [GRCh38] Chr9:117063419 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3879+18G>A | single nucleotide variant | not provided [RCV003695932] | Chr9:114282582 [GRCh38] Chr9:117044862 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1909-15T>C | single nucleotide variant | not provided [RCV003738849] | Chr9:114178276 [GRCh38] Chr9:116940556 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2748C>A (p.Gly916=) | single nucleotide variant | not provided [RCV003696005] | Chr9:114240240 [GRCh38] Chr9:117002520 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.951A>G (p.Pro317=) | single nucleotide variant | not provided [RCV003689111] | Chr9:114168506 [GRCh38] Chr9:116930786 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4585-12T>C | single nucleotide variant | not provided [RCV003662060] | Chr9:114300058 [GRCh38] Chr9:117062338 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2466+15G>C | single nucleotide variant | not provided [RCV003574481] | Chr9:114222282 [GRCh38] Chr9:116984562 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4938+11G>A | single nucleotide variant | not provided [RCV003578330] | Chr9:114304684 [GRCh38] Chr9:117066964 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2268+17C>T | single nucleotide variant | not provided [RCV003876958] | Chr9:114206313 [GRCh38] Chr9:116968593 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1677T>C (p.Pro559=) | single nucleotide variant | not provided [RCV003661459] | Chr9:114169232 [GRCh38] Chr9:116931512 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2016+20G>A | single nucleotide variant | not provided [RCV003739353] | Chr9:114183095 [GRCh38] Chr9:116945375 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-15G>C | single nucleotide variant | not provided [RCV003692035] | Chr9:114250600 [GRCh38] Chr9:117012880 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3594A>T (p.Gly1198=) | single nucleotide variant | not provided [RCV003687693] | Chr9:114270766 [GRCh38] Chr9:117033046 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4638+9T>C | single nucleotide variant | not provided [RCV003661535] | Chr9:114300132 [GRCh38] Chr9:117062412 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2125-16C>G | single nucleotide variant | not provided [RCV003574538] | Chr9:114205086 [GRCh38] Chr9:116967366 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2214T>C (p.Pro738=) | single nucleotide variant | not provided [RCV003695438] | Chr9:114205803 [GRCh38] Chr9:116968083 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2466+11T>C | single nucleotide variant | not provided [RCV003665987] | Chr9:114222278 [GRCh38] Chr9:116984558 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2565+17C>A | single nucleotide variant | not provided [RCV003715718] | Chr9:114231883 [GRCh38] Chr9:116994163 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3033+17G>T | single nucleotide variant | not provided [RCV003881977] | Chr9:114250685 [GRCh38] Chr9:117012965 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1830G>T (p.Ser610=) | single nucleotide variant | not provided [RCV003659905] | Chr9:114169385 [GRCh38] Chr9:116931665 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3880-12C>T | single nucleotide variant | not provided [RCV003573590] | Chr9:114283697 [GRCh38] Chr9:117045977 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3034-9C>T | single nucleotide variant | not provided [RCV003876520] | Chr9:114252584 [GRCh38] Chr9:117014864 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4770C>T (p.Asp1590=) | single nucleotide variant | not provided [RCV003544327] | Chr9:114301298 [GRCh38] Chr9:117063578 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1506G>C (p.Arg502=) | single nucleotide variant | not provided [RCV003688193] | Chr9:114169061 [GRCh38] Chr9:116931341 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5202C>G (p.Pro1734=) | single nucleotide variant | not provided [RCV003547178] | Chr9:114307763 [GRCh38] Chr9:117070043 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1314C>T (p.Pro438=) | single nucleotide variant | not provided [RCV003878034] | Chr9:114168869 [GRCh38] Chr9:116931149 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.903_916del (p.Gln301fs) | deletion | not provided [RCV003692693] | Chr9:114168451..114168464 [GRCh38] Chr9:116930731..116930744 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1698C>G (p.Val566=) | single nucleotide variant | not provided [RCV003690836] | Chr9:114169253 [GRCh38] Chr9:116931533 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4845+17T>C | single nucleotide variant | not provided [RCV003713319] | Chr9:114301734 [GRCh38] Chr9:117064014 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2736A>G (p.Pro912=) | single nucleotide variant | not provided [RCV003714571] | Chr9:114240228 [GRCh38] Chr9:117002508 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4044+23_4044+31del | deletion | not provided [RCV003876643] | Chr9:114288531..114288539 [GRCh38] Chr9:117050811..117050819 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4152+7G>A | single nucleotide variant | not provided [RCV003690370] | Chr9:114288974 [GRCh38] Chr9:117051254 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3108T>C (p.Gly1036=) | single nucleotide variant | not provided [RCV003693094] | Chr9:114252899 [GRCh38] Chr9:117015179 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4755+20A>G | single nucleotide variant | not provided [RCV003825599] | Chr9:114301145 [GRCh38] Chr9:117063425 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2881-13C>G | single nucleotide variant | not provided [RCV003544576] | Chr9:114243494 [GRCh38] Chr9:117005774 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5436+9C>T | single nucleotide variant | not provided [RCV003544747] | Chr9:114309487 [GRCh38] Chr9:117071767 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1995C>A (p.Leu665=) | single nucleotide variant | not provided [RCV003662907] | Chr9:114183054 [GRCh38] Chr9:116945334 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2172G>T (p.Gly724=) | single nucleotide variant | not provided [RCV003573091] | Chr9:114205761 [GRCh38] Chr9:116968041 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.63-11C>G | single nucleotide variant | not provided [RCV003715184] | Chr9:114162704 [GRCh38] Chr9:116924984 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4584+2T>A | single nucleotide variant | not provided [RCV003692049] | Chr9:114292212 [GRCh38] Chr9:117054492 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.2565+16C>G | single nucleotide variant | not provided [RCV003827247] | Chr9:114231882 [GRCh38] Chr9:116994162 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4638+15G>T | single nucleotide variant | not provided [RCV003687673] | Chr9:114300138 [GRCh38] Chr9:117062418 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2502G>T (p.Pro834=) | single nucleotide variant | not provided [RCV003713827] | Chr9:114231114 [GRCh38] Chr9:116993394 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.62+17G>T | single nucleotide variant | not provided [RCV003547920] | Chr9:114156029 [GRCh38] Chr9:116918309 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2010A>G (p.Gly670=) | single nucleotide variant | not provided [RCV003692406] | Chr9:114183069 [GRCh38] Chr9:116945349 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4099-15C>T | single nucleotide variant | not provided [RCV003880666] | Chr9:114288899 [GRCh38] Chr9:117051179 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.63-18G>T | single nucleotide variant | not provided [RCV003573024] | Chr9:114162697 [GRCh38] Chr9:116924977 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3705C>T (p.Val1235=) | single nucleotide variant | not provided [RCV003573287] | Chr9:114275756 [GRCh38] Chr9:117038036 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4872+11_4872+12del | deletion | not provided [RCV003692066] | Chr9:114302118..114302119 [GRCh38] Chr9:117064398..117064399 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5218-12G>T | single nucleotide variant | not provided [RCV003686608] | Chr9:114309248 [GRCh38] Chr9:117071528 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1864C>T (p.Leu622=) | single nucleotide variant | not provided [RCV003692880] | Chr9:114169419 [GRCh38] Chr9:116931699 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4713C>T (p.Gly1571=) | single nucleotide variant | not provided [RCV003692881] | Chr9:114301083 [GRCh38] Chr9:117063363 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5129del (p.Asn1710fs) | deletion | not provided [RCV003572205] | Chr9:114307688 [GRCh38] Chr9:117069968 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2190C>T (p.Gly730=) | single nucleotide variant | not provided [RCV003716345] | Chr9:114205779 [GRCh38] Chr9:116968059 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4260+14G>C | single nucleotide variant | not provided [RCV003882307] | Chr9:114290125 [GRCh38] Chr9:117052405 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5436+20C>G | single nucleotide variant | not provided [RCV003687868] | Chr9:114309498 [GRCh38] Chr9:117071778 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.134-8C>T | single nucleotide variant | not provided [RCV003714199] | Chr9:114167681 [GRCh38] Chr9:116929961 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5199G>A (p.Lys1733=) | single nucleotide variant | not provided [RCV003714212] | Chr9:114307760 [GRCh38] Chr9:117070040 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3339+20G>A | single nucleotide variant | not provided [RCV003575721] | Chr9:114265130 [GRCh38] Chr9:117027410 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5061C>G (p.Ala1687=) | single nucleotide variant | not provided [RCV003544139] | Chr9:114306642 [GRCh38] Chr9:117068922 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5436+10A>G | single nucleotide variant | not provided [RCV003665853] | Chr9:114309488 [GRCh38] Chr9:117071768 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4872+19C>T | single nucleotide variant | not provided [RCV003717650] | Chr9:114302127 [GRCh38] Chr9:117064407 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3738G>C (p.Gly1246=) | single nucleotide variant | not provided [RCV003835373] | Chr9:114282297 [GRCh38] Chr9:117044577 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2421+15T>A | single nucleotide variant | not provided [RCV003579581] | Chr9:114219859 [GRCh38] Chr9:116982139 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4939-16C>A | single nucleotide variant | not provided [RCV003852387] | Chr9:114306504 [GRCh38] Chr9:117068784 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.133+9C>T | single nucleotide variant | not provided [RCV003850510] | Chr9:114162794 [GRCh38] Chr9:116925074 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5436+17C>T | single nucleotide variant | not provided [RCV003550035] | Chr9:114309495 [GRCh38] Chr9:117071775 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4846-20C>A | single nucleotide variant | not provided [RCV003659018] | Chr9:114302062 [GRCh38] Chr9:117064342 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3642A>G (p.Glu1214=) | single nucleotide variant | not provided [RCV003697040] | Chr9:114275693 [GRCh38] Chr9:117037973 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4873-15C>T | single nucleotide variant | not provided [RCV003663655] | Chr9:114304593 [GRCh38] Chr9:117066873 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4098+16C>T | single nucleotide variant | not provided [RCV003832268] | Chr9:114288771 [GRCh38] Chr9:117051051 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3555+10del | deletion | not provided [RCV003834281] | Chr9:114269303 [GRCh38] Chr9:117031583 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3249+16A>C | single nucleotide variant | not provided [RCV003850743] | Chr9:114264424 [GRCh38] Chr9:117026704 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4756-17G>T | single nucleotide variant | not provided [RCV003850867] | Chr9:114301267 [GRCh38] Chr9:117063547 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3879+12C>G | single nucleotide variant | not provided [RCV003659363] | Chr9:114282576 [GRCh38] Chr9:117044856 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4044+10_4044+11insG | insertion | not provided [RCV003697403] | Chr9:114288521..114288522 [GRCh38] Chr9:117050801..117050802 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4206+11C>T | single nucleotide variant | not provided [RCV003557995] | Chr9:114289306 [GRCh38] Chr9:117051586 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2125-16C>T | single nucleotide variant | not provided [RCV003659491] | Chr9:114205086 [GRCh38] Chr9:116967366 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5436+19C>T | single nucleotide variant | not provided [RCV003664113] | Chr9:114309497 [GRCh38] Chr9:117071777 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.558C>T (p.His186=) | single nucleotide variant | not provided [RCV003701242] | Chr9:114168113 [GRCh38] Chr9:116930393 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-5del | deletion | not provided [RCV003699281] | Chr9:114250610 [GRCh38] Chr9:117012890 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2422-14C>T | single nucleotide variant | not provided [RCV003674374] | Chr9:114222209 [GRCh38] Chr9:116984489 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.90C>G (p.Val30=) | single nucleotide variant | not provided [RCV003836705] | Chr9:114162742 [GRCh38] Chr9:116925022 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5437-7C>T | single nucleotide variant | not provided [RCV003672117] | Chr9:114310542 [GRCh38] Chr9:117072822 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1026C>A (p.Gly342=) | single nucleotide variant | not provided [RCV003658963] | Chr9:114168581 [GRCh38] Chr9:116930861 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5442A>G (p.Gln1814=) | single nucleotide variant | not provided [RCV003673485] | Chr9:114310554 [GRCh38] Chr9:117072834 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2124+2T>C | single nucleotide variant | not provided [RCV003670370] | Chr9:114196014 [GRCh38] Chr9:116958294 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.62+12C>T | single nucleotide variant | not provided [RCV003832455] | Chr9:114156024 [GRCh38] Chr9:116918304 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2979+17C>G | single nucleotide variant | not provided [RCV003814309] | Chr9:114245927 [GRCh38] Chr9:117008207 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3718-12C>T | single nucleotide variant | not provided [RCV003670223] | Chr9:114282265 [GRCh38] Chr9:117044545 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-8C>A | single nucleotide variant | not provided [RCV003856261] | Chr9:114290216 [GRCh38] Chr9:117052496 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4755+13A>T | single nucleotide variant | not provided [RCV003580201] | Chr9:114301138 [GRCh38] Chr9:117063418 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4206+20A>C | single nucleotide variant | not provided [RCV003659013] | Chr9:114289315 [GRCh38] Chr9:117051595 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2934+19C>A | single nucleotide variant | not provided [RCV003700495] | Chr9:114243579 [GRCh38] Chr9:117005859 [GRCh37] Chr9:9q32 |
likely benign |
NC_000009.12:g.114162718del | deletion | not provided [RCV003835188] | Chr9:114162714 [GRCh38] Chr9:116924994 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1962+17T>C | single nucleotide variant | not provided [RCV003561957] | Chr9:114178361 [GRCh38] Chr9:116940641 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1962+20C>T | single nucleotide variant | not provided [RCV003671381] | Chr9:114178364 [GRCh38] Chr9:116940644 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3087+18A>G | single nucleotide variant | not provided [RCV003560199] | Chr9:114252664 [GRCh38] Chr9:117014944 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3310C>T (p.Arg1104Ter) | single nucleotide variant | not provided [RCV003664611] | Chr9:114265081 [GRCh38] Chr9:117027361 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4873-3C>T | single nucleotide variant | not provided [RCV003817414] | Chr9:114304605 [GRCh38] Chr9:117066885 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.1962+16C>G | single nucleotide variant | not provided [RCV003725100] | Chr9:114178360 [GRCh38] Chr9:116940640 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3394-13G>C | single nucleotide variant | not provided [RCV003579753] | Chr9:114266552 [GRCh38] Chr9:117028832 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3501+17G>C | single nucleotide variant | not provided [RCV003670446] | Chr9:114267574 [GRCh38] Chr9:117029854 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2016+9_2016+19dup | duplication | not provided [RCV003549720] | Chr9:114183081..114183082 [GRCh38] Chr9:116945361..116945362 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3880-15C>G | single nucleotide variant | not provided [RCV003670046] | Chr9:114283694 [GRCh38] Chr9:117045974 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4939-15C>A | single nucleotide variant | not provided [RCV003703440] | Chr9:114306505 [GRCh38] Chr9:117068785 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4143G>A (p.Gln1381=) | single nucleotide variant | not provided [RCV003717774] | Chr9:114288958 [GRCh38] Chr9:117051238 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4207-4T>G | single nucleotide variant | not provided [RCV003579904] | Chr9:114290054 [GRCh38] Chr9:117052334 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.489C>A (p.Leu163=) | single nucleotide variant | not provided [RCV003702602] | Chr9:114168044 [GRCh38] Chr9:116930324 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3555+14A>G | single nucleotide variant | not provided [RCV003703344] | Chr9:114269308 [GRCh38] Chr9:117031588 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4585-11T>C | single nucleotide variant | not provided [RCV003697219] | Chr9:114300059 [GRCh38] Chr9:117062339 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3295-13C>T | single nucleotide variant | not provided [RCV003549353] | Chr9:114265053 [GRCh38] Chr9:117027333 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3609+12T>C | single nucleotide variant | not provided [RCV003699235] | Chr9:114270793 [GRCh38] Chr9:117033073 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5107+23del | deletion | not provided [RCV003811181] | Chr9:114306707 [GRCh38] Chr9:117068987 [GRCh37] Chr9:9q32 |
benign |
NM_032888.4(COL27A1):c.3717+17C>T | single nucleotide variant | not provided [RCV003726588] | Chr9:114275785 [GRCh38] Chr9:117038065 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2979+12A>G | single nucleotide variant | not provided [RCV003560650] | Chr9:114245922 [GRCh38] Chr9:117008202 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2836-6T>C | single nucleotide variant | not provided [RCV003579958] | Chr9:114242181 [GRCh38] Chr9:117004461 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3448-16T>C | single nucleotide variant | not provided [RCV003717704] | Chr9:114267488 [GRCh38] Chr9:117029768 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4846-17G>T | single nucleotide variant | not provided [RCV003561581] | Chr9:114302065 [GRCh38] Chr9:117064345 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2782-6C>T | single nucleotide variant | not provided [RCV003726677] | Chr9:114240428 [GRCh38] Chr9:117002708 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4845+20G>A | single nucleotide variant | not provided [RCV003811358] | Chr9:114301737 [GRCh38] Chr9:117064017 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3142-17C>T | single nucleotide variant | not provided [RCV003834986] | Chr9:114258524 [GRCh38] Chr9:117020804 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2836-15G>A | single nucleotide variant | not provided [RCV003669795] | Chr9:114242172 [GRCh38] Chr9:117004452 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1746C>T (p.Pro582=) | single nucleotide variant | not provided [RCV003702338] | Chr9:114169301 [GRCh38] Chr9:116931581 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2781+16G>C | single nucleotide variant | not provided [RCV003550190] | Chr9:114240289 [GRCh38] Chr9:117002569 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3249+18C>G | single nucleotide variant | not provided [RCV003670010] | Chr9:114264426 [GRCh38] Chr9:117026706 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2367+15T>C | single nucleotide variant | not provided [RCV003838353] | Chr9:114211041 [GRCh38] Chr9:116973321 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4542G>A (p.Gly1514=) | single nucleotide variant | not provided [RCV003726647] | Chr9:114292168 [GRCh38] Chr9:117054448 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3988-18C>T | single nucleotide variant | not provided [RCV003558347] | Chr9:114288437 [GRCh38] Chr9:117050717 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2565+1G>A | single nucleotide variant | not provided [RCV003560053] | Chr9:114231867 [GRCh38] Chr9:116994147 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4476+20A>G | single nucleotide variant | not provided [RCV003725265] | Chr9:114290937 [GRCh38] Chr9:117053217 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.921C>T (p.Asn307=) | single nucleotide variant | not provided [RCV003725316] | Chr9:114168476 [GRCh38] Chr9:116930756 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3880-15CTC[2] | microsatellite | not provided [RCV003840058] | Chr9:114283694..114283696 [GRCh38] Chr9:117045974..117045976 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2934+14G>A | single nucleotide variant | not provided [RCV003703302] | Chr9:114243574 [GRCh38] Chr9:117005854 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3196-16C>T | single nucleotide variant | not provided [RCV003701718] | Chr9:114264339 [GRCh38] Chr9:117026619 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4153-13C>T | single nucleotide variant | not provided [RCV003725333] | Chr9:114289229 [GRCh38] Chr9:117051509 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2070+8T>C | single nucleotide variant | not provided [RCV003673247] | Chr9:114194465 [GRCh38] Chr9:116956745 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2016+7_2016+10del | deletion | not provided [RCV003560182] | Chr9:114183081..114183084 [GRCh38] Chr9:116945361..116945364 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4932G>A (p.Arg1644=) | single nucleotide variant | not provided [RCV003816935] | Chr9:114304667 [GRCh38] Chr9:117066947 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3157C>T (p.Arg1053Ter) | single nucleotide variant | not provided [RCV003839373] | Chr9:114258556 [GRCh38] Chr9:117020836 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1909-13G>A | single nucleotide variant | not provided [RCV003815092] | Chr9:114178278 [GRCh38] Chr9:116940558 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1963-9C>T | single nucleotide variant | not provided [RCV003724054] | Chr9:114183013 [GRCh38] Chr9:116945293 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4305G>A (p.Gln1435=) | single nucleotide variant | not provided [RCV003701860] | Chr9:114290268 [GRCh38] Chr9:117052548 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4701+12C>A | single nucleotide variant | not provided [RCV003702685] | Chr9:114300699 [GRCh38] Chr9:117062979 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3687C>T (p.Pro1229=) | single nucleotide variant | not provided [RCV003669521] | Chr9:114275738 [GRCh38] Chr9:117038018 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2754T>C (p.Pro918=) | single nucleotide variant | not provided [RCV003699470] | Chr9:114240246 [GRCh38] Chr9:117002526 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2836-18C>G | single nucleotide variant | not provided [RCV003669548] | Chr9:114242169 [GRCh38] Chr9:117004449 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4701+14C>T | single nucleotide variant | not provided [RCV003835325] | Chr9:114300701 [GRCh38] Chr9:117062981 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4845+20G>T | single nucleotide variant | not provided [RCV003814198] | Chr9:114301737 [GRCh38] Chr9:117064017 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4369-19C>A | single nucleotide variant | not provided [RCV003559556] | Chr9:114290791 [GRCh38] Chr9:117053071 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2520+13T>A | single nucleotide variant | not provided [RCV003855747] | Chr9:114231145 [GRCh38] Chr9:116993425 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2880+7G>T | single nucleotide variant | not provided [RCV003725893] | Chr9:114242238 [GRCh38] Chr9:117004518 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1740C>G (p.Pro580=) | single nucleotide variant | not provided [RCV003815190] | Chr9:114169295 [GRCh38] Chr9:116931575 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-19C>T | single nucleotide variant | not provided [RCV003671696] | Chr9:114290205 [GRCh38] Chr9:117052485 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4639-14T>G | single nucleotide variant | not provided [RCV003699556] | Chr9:114300611 [GRCh38] Chr9:117062891 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.162C>T (p.Leu54=) | single nucleotide variant | not provided [RCV003717645] | Chr9:114167717 [GRCh38] Chr9:116929997 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2421+12A>C | single nucleotide variant | not provided [RCV003702635] | Chr9:114219856 [GRCh38] Chr9:116982136 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1557A>G (p.Thr519=) | single nucleotide variant | not provided [RCV003726019] | Chr9:114169112 [GRCh38] Chr9:116931392 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2323-17_2323-16del | deletion | not provided [RCV003723445] | Chr9:114210965..114210966 [GRCh38] Chr9:116973245..116973246 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4873-11T>C | single nucleotide variant | not provided [RCV003854860] | Chr9:114304597 [GRCh38] Chr9:117066877 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3555+16T>G | single nucleotide variant | not provided [RCV003817560] | Chr9:114269310 [GRCh38] Chr9:117031590 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2269-19C>G | single nucleotide variant | not provided [RCV003835783] | Chr9:114209656 [GRCh38] Chr9:116971936 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.504C>G (p.Val168=) | single nucleotide variant | not provided [RCV003814549] | Chr9:114168059 [GRCh38] Chr9:116930339 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-9A>G | single nucleotide variant | not provided [RCV003701352] | Chr9:114290215 [GRCh38] Chr9:117052495 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2367+14G>C | single nucleotide variant | not provided [RCV003697509] | Chr9:114211040 [GRCh38] Chr9:116973320 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5107+19G>A | single nucleotide variant | not provided [RCV003726070] | Chr9:114306707 [GRCh38] Chr9:117068987 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3933+15C>A | single nucleotide variant | not provided [RCV003814489] | Chr9:114283777 [GRCh38] Chr9:117046057 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1164C>T (p.Thr388=) | single nucleotide variant | not provided [RCV003726544] | Chr9:114168719 [GRCh38] Chr9:116930999 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1758C>T (p.Thr586=) | single nucleotide variant | not provided [RCV003701592] | Chr9:114169313 [GRCh38] Chr9:116931593 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3771+17G>T | single nucleotide variant | not provided [RCV003560747] | Chr9:114282347 [GRCh38] Chr9:117044627 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.174G>A (p.Lys58=) | single nucleotide variant | not provided [RCV003668327] | Chr9:114167729 [GRCh38] Chr9:116930009 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2826G>A (p.Leu942=) | single nucleotide variant | not provided [RCV003838960] | Chr9:114240478 [GRCh38] Chr9:117002758 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5283G>A (p.Gln1761=) | single nucleotide variant | not provided [RCV003580016] | Chr9:114309325 [GRCh38] Chr9:117071605 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3450G>A (p.Gly1150=) | single nucleotide variant | not provided [RCV003665914] | Chr9:114267506 [GRCh38] Chr9:117029786 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4842C>T (p.Pro1614=) | single nucleotide variant | not provided [RCV003668961] | Chr9:114301714 [GRCh38] Chr9:117063994 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4968G>C (p.Leu1656=) | single nucleotide variant | not provided [RCV003699355] | Chr9:114306549 [GRCh38] Chr9:117068829 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5108-16C>T | single nucleotide variant | not provided [RCV003701851] | Chr9:114307653 [GRCh38] Chr9:117069933 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.693C>T (p.His231=) | single nucleotide variant | not provided [RCV003672202] | Chr9:114168248 [GRCh38] Chr9:116930528 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2268+16C>T | single nucleotide variant | not provided [RCV003548846] | Chr9:114206312 [GRCh38] Chr9:116968592 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5478G>T (p.Arg1826=) | single nucleotide variant | not provided [RCV003699910] | Chr9:114310590 [GRCh38] Chr9:117072870 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4146C>A (p.Gly1382=) | single nucleotide variant | not provided [RCV003717174] | Chr9:114288961 [GRCh38] Chr9:117051241 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3735A>G (p.Ser1245=) | single nucleotide variant | not provided [RCV003548752] | Chr9:114282294 [GRCh38] Chr9:117044574 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4047C>T (p.Gly1349=) | single nucleotide variant | not provided [RCV003723660] | Chr9:114288704 [GRCh38] Chr9:117050984 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3288A>G (p.Gly1096=) | single nucleotide variant | not provided [RCV003659244] | Chr9:114264962 [GRCh38] Chr9:117027242 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.134-5C>T | single nucleotide variant | not provided [RCV003558168] | Chr9:114167684 [GRCh38] Chr9:116929964 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2170-20T>G | single nucleotide variant | not provided [RCV003670897] | Chr9:114205739 [GRCh38] Chr9:116968019 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5552G>A (p.Arg1851His) | single nucleotide variant | not provided [RCV003559950] | Chr9:114310664 [GRCh38] Chr9:117072944 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4584+14A>G | single nucleotide variant | not provided [RCV003668263] | Chr9:114292224 [GRCh38] Chr9:117054504 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3195+16C>T | single nucleotide variant | not provided [RCV003559956] | Chr9:114258610 [GRCh38] Chr9:117020890 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3555+11G>C | single nucleotide variant | not provided [RCV003834282] | Chr9:114269305 [GRCh38] Chr9:117031585 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2467-11T>C | single nucleotide variant | not provided [RCV003558270] | Chr9:114231068 [GRCh38] Chr9:116993348 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1774T>C (p.Leu592=) | single nucleotide variant | not provided [RCV003724251] | Chr9:114169329 [GRCh38] Chr9:116931609 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3610-4C>G | single nucleotide variant | not provided [RCV003701642] | Chr9:114275657 [GRCh38] Chr9:117037937 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3717+16C>G | single nucleotide variant | not provided [RCV003700487] | Chr9:114275784 [GRCh38] Chr9:117038064 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.624G>A (p.Gln208=) | single nucleotide variant | not provided [RCV003668842] | Chr9:114168179 [GRCh38] Chr9:116930459 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2935-18C>T | single nucleotide variant | not provided [RCV003579802] | Chr9:114245848 [GRCh38] Chr9:117008128 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4939-9T>A | single nucleotide variant | not provided [RCV003549186] | Chr9:114306511 [GRCh38] Chr9:117068791 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2935-4G>C | single nucleotide variant | not provided [RCV003666470] | Chr9:114245862 [GRCh38] Chr9:117008142 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3693C>T (p.Gly1231=) | single nucleotide variant | not provided [RCV003668023] | Chr9:114275744 [GRCh38] Chr9:117038024 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3156T>C (p.Ser1052=) | single nucleotide variant | not provided [RCV003668721] | Chr9:114258555 [GRCh38] Chr9:117020835 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3339+2T>C | single nucleotide variant | not provided [RCV003580306] | Chr9:114265112 [GRCh38] Chr9:117027392 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.1806C>T (p.Pro602=) | single nucleotide variant | not provided [RCV003665719] | Chr9:114169361 [GRCh38] Chr9:116931641 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4207-2del | deletion | not provided [RCV003558202] | Chr9:114290056 [GRCh38] Chr9:117052336 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4944C>T (p.Tyr1648=) | single nucleotide variant | not provided [RCV003568684] | Chr9:114306525 [GRCh38] Chr9:117068805 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3610-20C>A | single nucleotide variant | not provided [RCV003861691] | Chr9:114275641 [GRCh38] Chr9:117037921 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4476+14del | deletion | not provided [RCV003729583] | Chr9:114290930 [GRCh38] Chr9:117053210 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3786_3787delinsCT (p.Gln1263Ter) | indel | not provided [RCV003550317] | Chr9:114282471..114282472 [GRCh38] Chr9:117044751..117044752 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.159C>G (p.Gly53=) | single nucleotide variant | not provided [RCV003566346] | Chr9:114167714 [GRCh38] Chr9:116929994 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2323-18C>T | single nucleotide variant | not provided [RCV003562507] | Chr9:114210964 [GRCh38] Chr9:116973244 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3447+13G>A | single nucleotide variant | not provided [RCV003562522] | Chr9:114266631 [GRCh38] Chr9:117028911 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.372G>T (p.Leu124=) | single nucleotide variant | not provided [RCV003728481] | Chr9:114167927 [GRCh38] Chr9:116930207 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2934+12T>C | single nucleotide variant | not provided [RCV003733544] | Chr9:114243572 [GRCh38] Chr9:117005852 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4939-11C>A | single nucleotide variant | not provided [RCV003563439] | Chr9:114306509 [GRCh38] Chr9:117068789 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4389G>C (p.Gly1463=) | single nucleotide variant | not provided [RCV003562656] | Chr9:114290830 [GRCh38] Chr9:117053110 [GRCh37] Chr9:9q32 |
likely benign |
NC_000009.12:g.114290059del | deletion | not provided [RCV003565085] | Chr9:114290057 [GRCh38] Chr9:117052337 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.5466C>G (p.Leu1822=) | single nucleotide variant | not provided [RCV003567772] | Chr9:114310578 [GRCh38] Chr9:117072858 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4702-17del | deletion | not provided [RCV003842896] | Chr9:114301054 [GRCh38] Chr9:117063334 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.612G>T (p.Pro204=) | single nucleotide variant | not provided [RCV003861948] | Chr9:114168167 [GRCh38] Chr9:116930447 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.585C>A (p.Gly195=) | single nucleotide variant | not provided [RCV003567005] | Chr9:114168140 [GRCh38] Chr9:116930420 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2160C>G (p.Pro720=) | single nucleotide variant | not provided [RCV003681829] | Chr9:114205137 [GRCh38] Chr9:116967417 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2781+13C>G | single nucleotide variant | not provided [RCV003727085] | Chr9:114240286 [GRCh38] Chr9:117002566 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3196-8dup | duplication | not provided [RCV003840939] | Chr9:114264346..114264347 [GRCh38] Chr9:117026626..117026627 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-4A>G | single nucleotide variant | not provided [RCV003709253] | Chr9:114250611 [GRCh38] Chr9:117012891 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4464C>G (p.Pro1488=) | single nucleotide variant | not provided [RCV003822932] | Chr9:114290905 [GRCh38] Chr9:117053185 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.24G>A (p.Gly8=) | single nucleotide variant | not provided [RCV003843648] | Chr9:114155974 [GRCh38] Chr9:116918254 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4846-15A>T | single nucleotide variant | not provided [RCV003550664] | Chr9:114302067 [GRCh38] Chr9:117064347 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4152+10G>T | single nucleotide variant | not provided [RCV003824261] | Chr9:114288977 [GRCh38] Chr9:117051257 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.63-16G>T | single nucleotide variant | not provided [RCV003678252] | Chr9:114162699 [GRCh38] Chr9:116924979 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1884A>G (p.Gly628=) | single nucleotide variant | not provided [RCV003846578] | Chr9:114169439 [GRCh38] Chr9:116931719 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2017-8T>C | single nucleotide variant | not provided [RCV003568743] | Chr9:114194396 [GRCh38] Chr9:116956676 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2727+19_2727+22dup | duplication | not provided [RCV003704380] | Chr9:114237733..114237734 [GRCh38] Chr9:117000013..117000014 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2346G>A (p.Lys782=) | single nucleotide variant | not provided [RCV003675655] | Chr9:114211005 [GRCh38] Chr9:116973285 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5107+13C>T | single nucleotide variant | not provided [RCV003729384] | Chr9:114306701 [GRCh38] Chr9:117068981 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4809+19A>G | single nucleotide variant | not provided [RCV003675102] | Chr9:114301481 [GRCh38] Chr9:117063761 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1758C>A (p.Thr586=) | single nucleotide variant | not provided [RCV003676359] | Chr9:114169313 [GRCh38] Chr9:116931593 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2223+17C>G | single nucleotide variant | not provided [RCV003676969] | Chr9:114205829 [GRCh38] Chr9:116968109 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2718T>C (p.Pro906=) | single nucleotide variant | not provided [RCV003554464] | Chr9:114237706 [GRCh38] Chr9:116999986 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4561G>T (p.Glu1521Ter) | single nucleotide variant | not provided [RCV003554496] | Chr9:114292187 [GRCh38] Chr9:117054467 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2323-16del | deletion | not provided [RCV003567481] | Chr9:114210966 [GRCh38] Chr9:116973246 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-5C>G | single nucleotide variant | not provided [RCV003674585] | Chr9:114290219 [GRCh38] Chr9:117052499 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4846-19C>A | single nucleotide variant | not provided [RCV003679817] | Chr9:114302063 [GRCh38] Chr9:117064343 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1963-15C>T | single nucleotide variant | not provided [RCV003865102] | Chr9:114183007 [GRCh38] Chr9:116945287 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2880+11C>A | single nucleotide variant | not provided [RCV003818649] | Chr9:114242242 [GRCh38] Chr9:117004522 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4584+10C>A | single nucleotide variant | not provided [RCV003551047] | Chr9:114292220 [GRCh38] Chr9:117054500 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1251_1252del (p.Arg417fs) | microsatellite | not provided [RCV003566514] | Chr9:114168804..114168805 [GRCh38] Chr9:116931084..116931085 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2368-7C>T | single nucleotide variant | not provided [RCV003681319] | Chr9:114219784 [GRCh38] Chr9:116982064 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3141+15C>T | single nucleotide variant | not provided [RCV003732520] | Chr9:114252947 [GRCh38] Chr9:117015227 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4045-17T>C | single nucleotide variant | not provided [RCV003820355] | Chr9:114288685 [GRCh38] Chr9:117050965 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5107+18C>G | single nucleotide variant | not provided [RCV003731392] | Chr9:114306706 [GRCh38] Chr9:117068986 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3933+20C>G | single nucleotide variant | not provided [RCV003736339] | Chr9:114283782 [GRCh38] Chr9:117046062 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2187G>A (p.Glu729=) | single nucleotide variant | not provided [RCV003541991] | Chr9:114205776 [GRCh38] Chr9:116968056 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1308A>G (p.Pro436=) | single nucleotide variant | not provided [RCV003555631] | Chr9:114168863 [GRCh38] Chr9:116931143 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4639-15C>A | single nucleotide variant | not provided [RCV003866296] | Chr9:114300610 [GRCh38] Chr9:117062890 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3142-15_3142-12del | deletion | not provided [RCV003736057] | Chr9:114258523..114258526 [GRCh38] Chr9:117020803..117020806 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4255del (p.Val1419fs) | deletion | not provided [RCV003858040] | Chr9:114290101 [GRCh38] Chr9:117052381 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3447+22_3447+30del | deletion | not provided [RCV003729368] | Chr9:114266638..114266646 [GRCh38] Chr9:117028918..117028926 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5325G>A (p.Glu1775=) | single nucleotide variant | not provided [RCV003818652] | Chr9:114309367 [GRCh38] Chr9:117071647 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2076C>T (p.Asp692=) | single nucleotide variant | not provided [RCV003705351] | Chr9:114195964 [GRCh38] Chr9:116958244 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1467A>G (p.Ser489=) | single nucleotide variant | not provided [RCV003552296] | Chr9:114169022 [GRCh38] Chr9:116931302 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5217+13T>C | single nucleotide variant | not provided [RCV003555632] | Chr9:114307791 [GRCh38] Chr9:117070071 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2619+12A>G | single nucleotide variant | not provided [RCV003676889] | Chr9:114235664 [GRCh38] Chr9:116997944 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3250-11G>A | single nucleotide variant | not provided [RCV003566010] | Chr9:114264913 [GRCh38] Chr9:117027193 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2520+19C>T | single nucleotide variant | not provided [RCV003566878] | Chr9:114231151 [GRCh38] Chr9:116993431 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4755+7G>A | single nucleotide variant | not provided [RCV003728223] | Chr9:114301132 [GRCh38] Chr9:117063412 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5217+17A>C | single nucleotide variant | not provided [RCV003563403] | Chr9:114307795 [GRCh38] Chr9:117070075 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1875G>A (p.Gly625=) | single nucleotide variant | not provided [RCV003563466] | Chr9:114169430 [GRCh38] Chr9:116931710 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3142-18T>C | single nucleotide variant | not provided [RCV003820556] | Chr9:114258523 [GRCh38] Chr9:117020803 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3339+18T>G | single nucleotide variant | not provided [RCV003731027] | Chr9:114265128 [GRCh38] Chr9:117027408 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1536G>C (p.Ser512=) | single nucleotide variant | not provided [RCV003552532] | Chr9:114169091 [GRCh38] Chr9:116931371 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2835+19C>G | single nucleotide variant | not provided [RCV003679445] | Chr9:114240506 [GRCh38] Chr9:117002786 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.399C>G (p.Gly133=) | single nucleotide variant | not provided [RCV003552766] | Chr9:114167954 [GRCh38] Chr9:116930234 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4869A>G (p.Gln1623=) | single nucleotide variant | not provided [RCV003841995] | Chr9:114302105 [GRCh38] Chr9:117064385 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.611dup (p.His205fs) | duplication | not provided [RCV003550383] | Chr9:114168163..114168164 [GRCh38] Chr9:116930443..116930444 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4275G>A (p.Leu1425=) | single nucleotide variant | not provided [RCV003682551] | Chr9:114290238 [GRCh38] Chr9:117052518 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5108-20C>A | single nucleotide variant | not provided [RCV003729359] | Chr9:114307649 [GRCh38] Chr9:117069929 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4494C>G (p.Pro1498=) | single nucleotide variant | not provided [RCV003551474] | Chr9:114292120 [GRCh38] Chr9:117054400 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2674-16C>T | single nucleotide variant | not provided [RCV003709440] | Chr9:114237646 [GRCh38] Chr9:116999926 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2782-15T>C | single nucleotide variant | not provided [RCV003719169] | Chr9:114240419 [GRCh38] Chr9:117002699 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2070+11A>C | single nucleotide variant | not provided [RCV003722028] | Chr9:114194468 [GRCh38] Chr9:116956748 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4680T>C (p.Pro1560=) | single nucleotide variant | not provided [RCV003551496] | Chr9:114300666 [GRCh38] Chr9:117062946 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4938+13G>T | single nucleotide variant | not provided [RCV003865174] | Chr9:114304686 [GRCh38] Chr9:117066966 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.134-14T>C | single nucleotide variant | not provided [RCV003728124] | Chr9:114167675 [GRCh38] Chr9:116929955 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2836-17G>A | single nucleotide variant | not provided [RCV003555532] | Chr9:114242170 [GRCh38] Chr9:117004450 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2227T>C (p.Leu743=) | single nucleotide variant | not provided [RCV003719310] | Chr9:114206255 [GRCh38] Chr9:116968535 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1963-16T>C | single nucleotide variant | not provided [RCV003684011] | Chr9:114183006 [GRCh38] Chr9:116945286 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2367+20A>G | single nucleotide variant | not provided [RCV003869379] | Chr9:114211046 [GRCh38] Chr9:116973326 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4939-9T>G | single nucleotide variant | not provided [RCV003685297] | Chr9:114306511 [GRCh38] Chr9:117068791 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1711C>T (p.Leu571=) | single nucleotide variant | not provided [RCV003542656] | Chr9:114169266 [GRCh38] Chr9:116931546 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2782-18T>G | single nucleotide variant | not provided [RCV003731110] | Chr9:114240416 [GRCh38] Chr9:117002696 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2727+13C>T | single nucleotide variant | not provided [RCV003733056] | Chr9:114237728 [GRCh38] Chr9:117000008 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2619+19C>T | single nucleotide variant | not provided [RCV003735018] | Chr9:114235671 [GRCh38] Chr9:116997951 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5108-12C>T | single nucleotide variant | not provided [RCV003555668] | Chr9:114307657 [GRCh38] Chr9:117069937 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3699T>C (p.Pro1233=) | single nucleotide variant | not provided [RCV003686128] | Chr9:114275750 [GRCh38] Chr9:117038030 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2832C>G (p.Pro944=) | single nucleotide variant | not provided [RCV003720586] | Chr9:114240484 [GRCh38] Chr9:117002764 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5436+16C>A | single nucleotide variant | not provided [RCV003722348] | Chr9:114309494 [GRCh38] Chr9:117071774 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4873-10C>T | single nucleotide variant | not provided [RCV003678636] | Chr9:114304598 [GRCh38] Chr9:117066878 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.192C>G (p.Pro64=) | single nucleotide variant | not provided [RCV003551970] | Chr9:114167747 [GRCh38] Chr9:116930027 [GRCh37] Chr9:9q32 |
likely benign |
NC_000009.12:g.114205103del | deletion | not provided [RCV003847137] | Chr9:114205101 [GRCh38] Chr9:116967381 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1692G>A (p.Arg564=) | single nucleotide variant | not provided [RCV003711765] | Chr9:114169247 [GRCh38] Chr9:116931527 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3034-7A>G | single nucleotide variant | not provided [RCV003737422] | Chr9:114252586 [GRCh38] Chr9:117014866 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2421+16C>G | single nucleotide variant | not provided [RCV003719419] | Chr9:114219860 [GRCh38] Chr9:116982140 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5218-11C>T | single nucleotide variant | not provided [RCV003722398] | Chr9:114309249 [GRCh38] Chr9:117071529 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4756-4G>A | single nucleotide variant | not provided [RCV003680713] | Chr9:114301280 [GRCh38] Chr9:117063560 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3033+16G>A | single nucleotide variant | not provided [RCV003555820] | Chr9:114250684 [GRCh38] Chr9:117012964 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2170-13T>C | single nucleotide variant | not provided [RCV003737534] | Chr9:114205746 [GRCh38] Chr9:116968026 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2268+13T>G | single nucleotide variant | not provided [RCV003737575] | Chr9:114206309 [GRCh38] Chr9:116968589 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3988-18C>G | single nucleotide variant | not provided [RCV003566685] | Chr9:114288437 [GRCh38] Chr9:117050717 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5437-10C>A | single nucleotide variant | not provided [RCV003566688] | Chr9:114310539 [GRCh38] Chr9:117072819 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.918A>C (p.Thr306=) | single nucleotide variant | not provided [RCV003552194] | Chr9:114168473 [GRCh38] Chr9:116930753 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.783G>A (p.Gln261=) | single nucleotide variant | not provided [RCV003566759] | Chr9:114168338 [GRCh38] Chr9:116930618 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5031G>A (p.Lys1677=) | single nucleotide variant | not provided [RCV003566760] | Chr9:114306612 [GRCh38] Chr9:117068892 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5280C>A (p.Thr1760=) | single nucleotide variant | not provided [RCV003733508] | Chr9:114309322 [GRCh38] Chr9:117071602 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4638+15G>A | single nucleotide variant | not provided [RCV003735567] | Chr9:114300138 [GRCh38] Chr9:117062418 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2070+19C>A | single nucleotide variant | not provided [RCV003735636] | Chr9:114194476 [GRCh38] Chr9:116956756 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4845+13G>C | single nucleotide variant | not provided [RCV003735637] | Chr9:114301730 [GRCh38] Chr9:117064010 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4569G>T (p.Gly1523=) | single nucleotide variant | not provided [RCV003684546] | Chr9:114292195 [GRCh38] Chr9:117054475 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5281C>T (p.Gln1761Ter) | single nucleotide variant | not provided [RCV003683923] | Chr9:114309323 [GRCh38] Chr9:117071603 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.1767C>G (p.Ala589=) | single nucleotide variant | not provided [RCV003719065] | Chr9:114169322 [GRCh38] Chr9:116931602 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2979+13C>G | single nucleotide variant | not provided [RCV003871194] | Chr9:114245923 [GRCh38] Chr9:117008203 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5437-20A>C | single nucleotide variant | not provided [RCV003562492] | Chr9:114310529 [GRCh38] Chr9:117072809 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1866G>C (p.Leu622=) | single nucleotide variant | not provided [RCV003676087] | Chr9:114169421 [GRCh38] Chr9:116931701 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1920G>C (p.Gly640=) | single nucleotide variant | not provided [RCV003552281] | Chr9:114178302 [GRCh38] Chr9:116940582 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2013C>G (p.Ala671=) | single nucleotide variant | not provided [RCV003552302] | Chr9:114183072 [GRCh38] Chr9:116945352 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2832C>A (p.Pro944=) | single nucleotide variant | not provided [RCV003686000] | Chr9:114240484 [GRCh38] Chr9:117002764 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3988-16G>A | single nucleotide variant | not provided [RCV003733843] | Chr9:114288439 [GRCh38] Chr9:117050719 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-15G>A | single nucleotide variant | not provided [RCV003737872] | Chr9:114250600 [GRCh38] Chr9:117012880 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3880-18G>T | single nucleotide variant | not provided [RCV003845751] | Chr9:114283691 [GRCh38] Chr9:117045971 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2224-14G>A | single nucleotide variant | not provided [RCV003733900] | Chr9:114206238 [GRCh38] Chr9:116968518 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1929G>A (p.Gly643=) | single nucleotide variant | not provided [RCV003867515] | Chr9:114178311 [GRCh38] Chr9:116940591 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2322+10C>T | single nucleotide variant | not provided [RCV003845797] | Chr9:114209738 [GRCh38] Chr9:116972018 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3340-8C>T | single nucleotide variant | not provided [RCV003854060] | Chr9:114265414 [GRCh38] Chr9:117027694 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3610-20C>T | single nucleotide variant | not provided [RCV003736099] | Chr9:114275641 [GRCh38] Chr9:117037921 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1962+14C>T | single nucleotide variant | not provided [RCV003867571] | Chr9:114178358 [GRCh38] Chr9:116940638 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2367+18C>A | single nucleotide variant | not provided [RCV003737615] | Chr9:114211044 [GRCh38] Chr9:116973324 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2881-9C>G | single nucleotide variant | not provided [RCV003719619] | Chr9:114243498 [GRCh38] Chr9:117005778 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5437-20A>G | single nucleotide variant | not provided [RCV003737657] | Chr9:114310529 [GRCh38] Chr9:117072809 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3244C>T (p.Leu1082=) | single nucleotide variant | not provided [RCV003871871] | Chr9:114264403 [GRCh38] Chr9:117026683 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2070+18C>T | single nucleotide variant | not provided [RCV003681687] | Chr9:114194475 [GRCh38] Chr9:116956755 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4153-12C>G | single nucleotide variant | not provided [RCV003871929] | Chr9:114289230 [GRCh38] Chr9:117051510 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3502-13C>T | single nucleotide variant | not provided [RCV003737905] | Chr9:114269228 [GRCh38] Chr9:117031508 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3295-12A>G | single nucleotide variant | not provided [RCV003721714] | Chr9:114265054 [GRCh38] Chr9:117027334 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1719C>T (p.Thr573=) | single nucleotide variant | not provided [RCV003841456] | Chr9:114169274 [GRCh38] Chr9:116931554 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-6C>T | single nucleotide variant | not provided [RCV003872072] | Chr9:114290218 [GRCh38] Chr9:117052498 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2070+13G>T | single nucleotide variant | not provided [RCV003730710] | Chr9:114194470 [GRCh38] Chr9:116956750 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5436+17C>G | single nucleotide variant | not provided [RCV003678136] | Chr9:114309495 [GRCh38] Chr9:117071775 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4872+20T>C | single nucleotide variant | not provided [RCV003555249] | Chr9:114302128 [GRCh38] Chr9:117064408 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.846G>A (p.Leu282=) | single nucleotide variant | not provided [RCV003719032] | Chr9:114168401 [GRCh38] Chr9:116930681 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2368-12C>T | single nucleotide variant | not provided [RCV003872160] | Chr9:114219779 [GRCh38] Chr9:116982059 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.633T>G (p.Gly211=) | single nucleotide variant | not provided [RCV003683716] | Chr9:114168188 [GRCh38] Chr9:116930468 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4618G>A (p.Ala1540Thr) | single nucleotide variant | not provided [RCV003719784] | Chr9:114300103 [GRCh38] Chr9:117062383 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2169+18A>G | single nucleotide variant | not provided [RCV003870468] | Chr9:114205164 [GRCh38] Chr9:116967444 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4756-13dup | duplication | not provided [RCV003565772] | Chr9:114301270..114301271 [GRCh38] Chr9:117063550..117063551 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2169+1G>T | single nucleotide variant | not provided [RCV003684713] | Chr9:114205147 [GRCh38] Chr9:116967427 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.4939-17C>A | single nucleotide variant | not provided [RCV003732530] | Chr9:114306503 [GRCh38] Chr9:117068783 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3196-8T>C | single nucleotide variant | not provided [RCV003684752] | Chr9:114264347 [GRCh38] Chr9:117026627 [GRCh37] Chr9:9q32 |
likely benign |
GRCh37/hg19 9q32(chr9:117037819-117102046)x1 | copy number loss | not specified [RCV003986841] | Chr9:117037819..117102046 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.3265C>T (p.Gln1089Ter) | single nucleotide variant | not provided [RCV003675485] | Chr9:114264939 [GRCh38] Chr9:117027219 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.3718-15C>T | single nucleotide variant | not provided [RCV003844568] | Chr9:114282262 [GRCh38] Chr9:117044542 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4369-11T>C | single nucleotide variant | not provided [RCV003567839] | Chr9:114290799 [GRCh38] Chr9:117053079 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-7C>A | single nucleotide variant | not provided [RCV003555163] | Chr9:114290217 [GRCh38] Chr9:117052497 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3078G>A (p.Lys1026=) | single nucleotide variant | not provided [RCV003867144] | Chr9:114252637 [GRCh38] Chr9:117014917 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4873-3del | deletion | not provided [RCV003722414] | Chr9:114304603 [GRCh38] Chr9:117066883 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3933+14A>C | single nucleotide variant | not provided [RCV003722511] | Chr9:114283776 [GRCh38] Chr9:117046056 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4044+13C>T | single nucleotide variant | not provided [RCV003729492] | Chr9:114288524 [GRCh38] Chr9:117050804 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2422-17TC[3] | microsatellite | not provided [RCV003860976] | Chr9:114222206..114222207 [GRCh38] Chr9:116984486..116984487 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1908+9G>A | single nucleotide variant | not provided [RCV003555246] | Chr9:114169472 [GRCh38] Chr9:116931752 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2421+19T>C | single nucleotide variant | not provided [RCV003555378] | Chr9:114219863 [GRCh38] Chr9:116982143 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3365del (p.Pro1122fs) | deletion | not provided [RCV003719103] | Chr9:114265442 [GRCh38] Chr9:117027722 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2071-20A>G | single nucleotide variant | not provided [RCV003737135] | Chr9:114195939 [GRCh38] Chr9:116958219 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3447+17C>G | single nucleotide variant | not provided [RCV003722497] | Chr9:114266635 [GRCh38] Chr9:117028915 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2367+15del | deletion | not provided [RCV003730966] | Chr9:114211041 [GRCh38] Chr9:116973321 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1702T>C (p.Leu568=) | single nucleotide variant | not provided [RCV003867261] | Chr9:114169257 [GRCh38] Chr9:116931537 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4098+20C>T | single nucleotide variant | not provided [RCV003719852] | Chr9:114288775 [GRCh38] Chr9:117051055 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3934-4G>A | single nucleotide variant | not provided [RCV003840686] | Chr9:114284720 [GRCh38] Chr9:117047000 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4261-11G>A | single nucleotide variant | not provided [RCV003737980] | Chr9:114290213 [GRCh38] Chr9:117052493 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2367+13C>T | single nucleotide variant | not provided [RCV003738019] | Chr9:114211039 [GRCh38] Chr9:116973319 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4830G>A (p.Gly1610=) | single nucleotide variant | not provided [RCV003685030] | Chr9:114301702 [GRCh38] Chr9:117063982 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2017-13G>T | single nucleotide variant | not provided [RCV003731106] | Chr9:114194391 [GRCh38] Chr9:116956671 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2422-9T>C | single nucleotide variant | not provided [RCV003566376] | Chr9:114222214 [GRCh38] Chr9:116984494 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3477C>G (p.Gly1159=) | single nucleotide variant | not provided [RCV003568367] | Chr9:114267533 [GRCh38] Chr9:117029813 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5217+12C>A | single nucleotide variant | not provided [RCV003719311] | Chr9:114307790 [GRCh38] Chr9:117070070 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2224-13T>C | single nucleotide variant | not provided [RCV003720249] | Chr9:114206239 [GRCh38] Chr9:116968519 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2724C>A (p.Pro908=) | single nucleotide variant | not provided [RCV003722990] | Chr9:114237712 [GRCh38] Chr9:116999992 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4792-10C>A | single nucleotide variant | not provided [RCV003841886] | Chr9:114301435 [GRCh38] Chr9:117063715 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3441A>T (p.Gly1147=) | single nucleotide variant | not provided [RCV003550437] | Chr9:114266612 [GRCh38] Chr9:117028892 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5427T>C (p.Asp1809=) | single nucleotide variant | not provided [RCV003853288] | Chr9:114309469 [GRCh38] Chr9:117071749 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2775C>T (p.Gly925=) | single nucleotide variant | not provided [RCV003737513] | Chr9:114240267 [GRCh38] Chr9:117002547 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4756-16C>T | single nucleotide variant | not provided [RCV003720271] | Chr9:114301268 [GRCh38] Chr9:117063548 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2323-19C>T | single nucleotide variant | not provided [RCV003869756] | Chr9:114210963 [GRCh38] Chr9:116973243 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4260+13A>G | single nucleotide variant | not provided [RCV003723155] | Chr9:114290124 [GRCh38] Chr9:117052404 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4891_4909del (p.Ala1631fs) | deletion | not provided [RCV003706465] | Chr9:114304626..114304644 [GRCh38] Chr9:117066906..117066924 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.4846-18_4846-16del | deletion | not provided [RCV003550648] | Chr9:114302063..114302065 [GRCh38] Chr9:117064343..117064345 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4846-18C>T | single nucleotide variant | not provided [RCV003737421] | Chr9:114302064 [GRCh38] Chr9:117064344 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2421+20G>C | single nucleotide variant | not provided [RCV003681022] | Chr9:114219864 [GRCh38] Chr9:116982144 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.62+20C>T | single nucleotide variant | not provided [RCV003737573] | Chr9:114156032 [GRCh38] Chr9:116918312 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3142-5C>T | single nucleotide variant | not provided [RCV003674912] | Chr9:114258536 [GRCh38] Chr9:117020816 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2223+10A>G | single nucleotide variant | not provided [RCV003818622] | Chr9:114205822 [GRCh38] Chr9:116968102 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1104C>G (p.Leu368=) | single nucleotide variant | not provided [RCV003864218] | Chr9:114168659 [GRCh38] Chr9:116930939 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1440A>G (p.Lys480=) | single nucleotide variant | not provided [RCV003721657] | Chr9:114168995 [GRCh38] Chr9:116931275 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4702-18C>T | single nucleotide variant | not provided [RCV003721656] | Chr9:114301054 [GRCh38] Chr9:117063334 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4638+14C>G | single nucleotide variant | not provided [RCV003562667] | Chr9:114300137 [GRCh38] Chr9:117062417 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2169+22del | deletion | not provided [RCV003842480] | Chr9:114205166 [GRCh38] Chr9:116967446 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4810-13C>G | single nucleotide variant | not provided [RCV003843864] | Chr9:114301669 [GRCh38] Chr9:117063949 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5439C>T (p.Val1813=) | single nucleotide variant | not provided [RCV003845853] | Chr9:114310551 [GRCh38] Chr9:117072831 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2835+14G>C | single nucleotide variant | not provided [RCV003864185] | Chr9:114240501 [GRCh38] Chr9:117002781 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2368-13T>G | single nucleotide variant | not provided [RCV003684408] | Chr9:114219778 [GRCh38] Chr9:116982058 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2299C>T (p.Leu767=) | single nucleotide variant | not provided [RCV003868937] | Chr9:114209705 [GRCh38] Chr9:116971985 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3034-13G>C | single nucleotide variant | not provided [RCV003862269] | Chr9:114252580 [GRCh38] Chr9:117014860 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2170-12G>A | single nucleotide variant | not provided [RCV003719630] | Chr9:114205747 [GRCh38] Chr9:116968027 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1563T>A (p.Pro521=) | single nucleotide variant | not provided [RCV003556986] | Chr9:114169118 [GRCh38] Chr9:116931398 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3699T>A (p.Pro1233=) | single nucleotide variant | not provided [RCV003557026] | Chr9:114275750 [GRCh38] Chr9:117038030 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3771+16T>C | single nucleotide variant | not provided [RCV003676689] | Chr9:114282346 [GRCh38] Chr9:117044626 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4845+15G>A | single nucleotide variant | not provided [RCV003736281] | Chr9:114301732 [GRCh38] Chr9:117064012 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5436+20C>T | single nucleotide variant | not provided [RCV003823688] | Chr9:114309498 [GRCh38] Chr9:117071778 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3501+20G>A | single nucleotide variant | not provided [RCV003679691] | Chr9:114267577 [GRCh38] Chr9:117029857 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.297A>G (p.Ala99=) | single nucleotide variant | not provided [RCV003733506] | Chr9:114167852 [GRCh38] Chr9:116930132 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.365G>A (p.Arg122His) | single nucleotide variant | not provided [RCV003733507] | Chr9:114167920 [GRCh38] Chr9:116930200 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.273T>G (p.Pro91=) | single nucleotide variant | not provided [RCV003555192] | Chr9:114167828 [GRCh38] Chr9:116930108 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-18del | deletion | not provided [RCV003734764] | Chr9:114250597 [GRCh38] Chr9:117012877 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1765G>T (p.Ala589Ser) | single nucleotide variant | not provided [RCV003842715] | Chr9:114169320 [GRCh38] Chr9:116931600 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.4756-14G>A | single nucleotide variant | not provided [RCV003735002] | Chr9:114301270 [GRCh38] Chr9:117063550 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.996A>C (p.Ala332=) | single nucleotide variant | not provided [RCV003865655] | Chr9:114168551 [GRCh38] Chr9:116930831 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4655T>C (p.Ile1552Thr) | single nucleotide variant | not provided [RCV003730654] | Chr9:114300641 [GRCh38] Chr9:117062921 [GRCh37] Chr9:9q32 |
uncertain significance |
NM_032888.4(COL27A1):c.2422-19G>A | single nucleotide variant | not provided [RCV003568375] | Chr9:114222204 [GRCh38] Chr9:116984484 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4809+9G>A | single nucleotide variant | not provided [RCV003823345] | Chr9:114301471 [GRCh38] Chr9:117063751 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.759C>T (p.Asp253=) | single nucleotide variant | not provided [RCV003732057] | Chr9:114168314 [GRCh38] Chr9:116930594 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2619+1G>T | single nucleotide variant | not provided [RCV003681023] | Chr9:114235653 [GRCh38] Chr9:116997933 [GRCh37] Chr9:9q32 |
likely pathogenic |
NM_032888.4(COL27A1):c.5218-18G>A | single nucleotide variant | not provided [RCV003676707] | Chr9:114309242 [GRCh38] Chr9:117071522 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2980-17G>T | single nucleotide variant | not provided [RCV003711449] | Chr9:114250598 [GRCh38] Chr9:117012878 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2880+16C>T | single nucleotide variant | not provided [RCV003734865] | Chr9:114242247 [GRCh38] Chr9:117004527 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4810-15C>T | single nucleotide variant | not provided [RCV003863854] | Chr9:114301667 [GRCh38] Chr9:117063947 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3447+11G>A | single nucleotide variant | not provided [RCV003733707] | Chr9:114266629 [GRCh38] Chr9:117028909 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3033+13G>C | single nucleotide variant | not provided [RCV003734887] | Chr9:114250681 [GRCh38] Chr9:117012961 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.192C>T (p.Pro64=) | single nucleotide variant | not provided [RCV003682243] | Chr9:114167747 [GRCh38] Chr9:116930027 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2520+10G>A | single nucleotide variant | not provided [RCV003852894] | Chr9:114231142 [GRCh38] Chr9:116993422 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3141+16G>A | single nucleotide variant | not provided [RCV003555645] | Chr9:114252948 [GRCh38] Chr9:117015228 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4099-4C>G | single nucleotide variant | not provided [RCV003555768] | Chr9:114288910 [GRCh38] Chr9:117051190 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3339+17C>A | single nucleotide variant | not provided [RCV003823428] | Chr9:114265127 [GRCh38] Chr9:117027407 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3543C>T (p.Leu1181=) | single nucleotide variant | not provided [RCV003710096] | Chr9:114269282 [GRCh38] Chr9:117031562 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.735A>T (p.Pro245=) | single nucleotide variant | not provided [RCV003847743] | Chr9:114168290 [GRCh38] Chr9:116930570 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3339+16T>C | single nucleotide variant | not provided [RCV003864927] | Chr9:114265126 [GRCh38] Chr9:117027406 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2125-17T>C | single nucleotide variant | not provided [RCV003705000] | Chr9:114205085 [GRCh38] Chr9:116967365 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2728-11C>T | single nucleotide variant | not provided [RCV003555724] | Chr9:114240209 [GRCh38] Chr9:117002489 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5124T>C (p.Asp1708=) | single nucleotide variant | not provided [RCV003707573] | Chr9:114307685 [GRCh38] Chr9:117069965 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2016+16A>C | single nucleotide variant | not provided [RCV003710451] | Chr9:114183091 [GRCh38] Chr9:116945371 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3423G>A (p.Gly1141=) | single nucleotide variant | not provided [RCV003563384] | Chr9:114266594 [GRCh38] Chr9:117028874 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4737G>A (p.Leu1579=) | single nucleotide variant | not provided [RCV003729389] | Chr9:114301107 [GRCh38] Chr9:117063387 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4300dup (p.Arg1434fs) | duplication | not provided [RCV003552883] | Chr9:114290262..114290263 [GRCh38] Chr9:117052542..117052543 [GRCh37] Chr9:9q32 |
pathogenic |
NM_032888.4(COL27A1):c.2934+15A>G | single nucleotide variant | not provided [RCV003552881] | Chr9:114243575 [GRCh38] Chr9:117005855 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3295-19C>A | single nucleotide variant | not provided [RCV003732343] | Chr9:114265047 [GRCh38] Chr9:117027327 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3934-17T>G | single nucleotide variant | not provided [RCV003841989] | Chr9:114284707 [GRCh38] Chr9:117046987 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3447+17C>T | single nucleotide variant | not provided [RCV003735659] | Chr9:114266635 [GRCh38] Chr9:117028915 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5556G>A (p.Leu1852=) | single nucleotide variant | not provided [RCV003567559] | Chr9:114310668 [GRCh38] Chr9:117072948 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4392C>T (p.Asp1464=) | single nucleotide variant | not provided [RCV003707391] | Chr9:114290833 [GRCh38] Chr9:117053113 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3294+16G>C | single nucleotide variant | not provided [RCV003675758] | Chr9:114264984 [GRCh38] Chr9:117027264 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4215G>A (p.Lys1405=) | single nucleotide variant | not provided [RCV003857092] | Chr9:114290066 [GRCh38] Chr9:117052346 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2727+19C>T | single nucleotide variant | not provided [RCV003820766] | Chr9:114237734 [GRCh38] Chr9:117000014 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4639-13C>T | single nucleotide variant | not provided [RCV003853683] | Chr9:114300612 [GRCh38] Chr9:117062892 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3198C>T (p.Gly1066=) | single nucleotide variant | not provided [RCV003858489] | Chr9:114264357 [GRCh38] Chr9:117026637 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2368-8C>A | single nucleotide variant | not provided [RCV003706359] | Chr9:114219783 [GRCh38] Chr9:116982063 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3250-15C>T | single nucleotide variant | not provided [RCV003735789] | Chr9:114264909 [GRCh38] Chr9:117027189 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1346C>T (p.Ser449Phe) | single nucleotide variant | not provided [RCV003735864] | Chr9:114168901 [GRCh38] Chr9:116931181 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4821C>T (p.Gly1607=) | single nucleotide variant | not provided [RCV003677180] | Chr9:114301693 [GRCh38] Chr9:117063973 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4369-7T>C | single nucleotide variant | not provided [RCV003678685] | Chr9:114290803 [GRCh38] Chr9:117053083 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2782-5C>T | single nucleotide variant | not provided [RCV003551511] | Chr9:114240429 [GRCh38] Chr9:117002709 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1209T>A (p.Thr403=) | single nucleotide variant | not provided [RCV003562504] | Chr9:114168764 [GRCh38] Chr9:116931044 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4206+11C>A | single nucleotide variant | not provided [RCV003840987] | Chr9:114289306 [GRCh38] Chr9:117051586 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3880-17G>T | single nucleotide variant | not provided [RCV003712257] | Chr9:114283692 [GRCh38] Chr9:117045972 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2674-6C>T | single nucleotide variant | not provided [RCV003566075] | Chr9:114237656 [GRCh38] Chr9:116999936 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1908+18C>T | single nucleotide variant | not provided [RCV003563908] | Chr9:114169481 [GRCh38] Chr9:116931761 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5445T>C (p.Asp1815=) | single nucleotide variant | not provided [RCV003564971] | Chr9:114310557 [GRCh38] Chr9:117072837 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2610A>G (p.Gln870=) | single nucleotide variant | not provided [RCV003680252] | Chr9:114235643 [GRCh38] Chr9:116997923 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2169+8C>G | single nucleotide variant | not provided [RCV003732786] | Chr9:114205154 [GRCh38] Chr9:116967434 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.636T>A (p.Ala212=) | single nucleotide variant | not provided [RCV003709561] | Chr9:114168191 [GRCh38] Chr9:116930471 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4368+15G>C | single nucleotide variant | not provided [RCV003846726] | Chr9:114290346 [GRCh38] Chr9:117052626 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4702-16T>C | single nucleotide variant | not provided [RCV003733016] | Chr9:114301056 [GRCh38] Chr9:117063336 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1719C>G (p.Thr573=) | single nucleotide variant | not provided [RCV003542856] | Chr9:114169274 [GRCh38] Chr9:116931554 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3333C>G (p.Gly1111=) | single nucleotide variant | not provided [RCV003566869] | Chr9:114265104 [GRCh38] Chr9:117027384 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3142-11C>T | single nucleotide variant | not provided [RCV003731013] | Chr9:114258530 [GRCh38] Chr9:117020810 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2979+15G>T | single nucleotide variant | not provided [RCV003731113] | Chr9:114245925 [GRCh38] Chr9:117008205 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2421+14G>A | single nucleotide variant | not provided [RCV003732906] | Chr9:114219858 [GRCh38] Chr9:116982138 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3448-14G>T | single nucleotide variant | not provided [RCV003678558] | Chr9:114267490 [GRCh38] Chr9:117029770 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.814T>C (p.Leu272=) | single nucleotide variant | not provided [RCV003566457] | Chr9:114168369 [GRCh38] Chr9:116930649 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3966T>A (p.Pro1322=) | single nucleotide variant | not provided [RCV003550632] | Chr9:114284756 [GRCh38] Chr9:117047036 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2169+16T>C | single nucleotide variant | not provided [RCV003565079] | Chr9:114205162 [GRCh38] Chr9:116967442 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.5214C>T (p.Ser1738=) | single nucleotide variant | not provided [RCV003556573] | Chr9:114307775 [GRCh38] Chr9:117070055 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.150G>A (p.Gln50=) | single nucleotide variant | not provided [RCV003565159] | Chr9:114167705 [GRCh38] Chr9:116929985 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3933+20C>T | single nucleotide variant | not provided [RCV003677411] | Chr9:114283782 [GRCh38] Chr9:117046062 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1017C>T (p.Ala339=) | single nucleotide variant | not provided [RCV003552496] | Chr9:114168572 [GRCh38] Chr9:116930852 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3549G>A (p.Gly1183=) | single nucleotide variant | not provided [RCV003568124] | Chr9:114269288 [GRCh38] Chr9:117031568 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3717+20G>A | single nucleotide variant | not provided [RCV003858730] | Chr9:114275788 [GRCh38] Chr9:117038068 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4965G>C (p.Val1655=) | single nucleotide variant | not provided [RCV003706687] | Chr9:114306546 [GRCh38] Chr9:117068826 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4584+11G>A | single nucleotide variant | not provided [RCV003729999] | Chr9:114292221 [GRCh38] Chr9:117054501 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2403T>C (p.Pro801=) | single nucleotide variant | not provided [RCV003552577] | Chr9:114219826 [GRCh38] Chr9:116982106 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1908+16G>T | single nucleotide variant | not provided [RCV003862053] | Chr9:114169479 [GRCh38] Chr9:116931759 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4638+12C>G | single nucleotide variant | not provided [RCV003848261] | Chr9:114300135 [GRCh38] Chr9:117062415 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3141+19A>G | single nucleotide variant | not provided [RCV003818811] | Chr9:114252951 [GRCh38] Chr9:117015231 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3319T>C (p.Leu1107=) | single nucleotide variant | not provided [RCV003708185] | Chr9:114265090 [GRCh38] Chr9:117027370 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.1638A>T (p.Gly546=) | single nucleotide variant | not provided [RCV003566665] | Chr9:114169193 [GRCh38] Chr9:116931473 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2520+17C>T | single nucleotide variant | not provided [RCV003728789] | Chr9:114231149 [GRCh38] Chr9:116993429 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4791+14C>G | single nucleotide variant | not provided [RCV003854175] | Chr9:114301333 [GRCh38] Chr9:117063613 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4639-9C>A | single nucleotide variant | not provided [RCV003677814] | Chr9:114300616 [GRCh38] Chr9:117062896 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4872+16_4872+27del | deletion | not provided [RCV003679664] | Chr9:114302121..114302132 [GRCh38] Chr9:117064401..117064412 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3609+20del | deletion | not provided [RCV003710140] | Chr9:114270801 [GRCh38] Chr9:117033081 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.2781+16G>A | single nucleotide variant | not provided [RCV003818882] | Chr9:114240289 [GRCh38] Chr9:117002569 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.3610-12C>A | single nucleotide variant | not provided [RCV003734521] | Chr9:114275649 [GRCh38] Chr9:117037929 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.4275G>T (p.Leu1425=) | single nucleotide variant | not provided [RCV003842852] | Chr9:114290238 [GRCh38] Chr9:117052518 [GRCh37] Chr9:9q32 |
likely benign |
NM_032888.4(COL27A1):c.966G>T (p.Leu322=) | single nucleotide variant | COL27A1-related condition [RCV003963981] | Chr9:114168521 [GRCh38] Chr9:116930801 [GRCh37] Chr9:9q32 |
likely benign |
The detailed report is available here: | Full Report | CSV | TAB | Printer | ||||
miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/). For more information about miRGate, see PMID:25858286 or access the full paper here. |
SHGC-80791 |
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SHGC-144392 |
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SHGC-144544 |
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SHGC-145671 |
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SHGC-145701 |
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SHGC-147982 |
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WI-22523 |
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SHGC-153772 |
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SHGC-156158 |
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SHGC-8827 |
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D1S1361 |
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alimentary part of gastrointestinal system | circulatory system | endocrine system | exocrine system | hemolymphoid system | hepatobiliary system | integumental system | musculoskeletal system | nervous system | renal system | reproductive system | respiratory system | sensory system | visual system | adipose tissue | appendage | entire extraembryonic component | pharyngeal arch | |
High | ||||||||||||||||||
Medium | 737 | 907 | 1060 | 355 | 103 | 349 | 2000 | 269 | 1166 | 211 | 984 | 921 | 15 | 423 | 1277 | 3 | ||
Low | 1667 | 1331 | 658 | 268 | 577 | 114 | 2348 | 1920 | 2479 | 183 | 459 | 627 | 159 | 1 | 781 | 1510 | 1 | 1 |
Below cutoff | 26 | 748 | 7 | 1046 | 2 | 8 | 7 | 82 | 24 | 17 | 58 | 1 | 1 | 1 |
RefSeq Transcripts | NG_034260 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_032888 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006717308 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006717310 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011519138 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011519140 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011519142 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011519143 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011519144 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011519145 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017015239 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047423992 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047423993 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047423994 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047423995 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364055 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364056 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364057 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364058 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364059 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364060 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364061 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364062 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364063 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364064 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364065 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364066 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054364067 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001746405 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_008488095 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_929860 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_929861 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_929862 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_929863 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AB058773 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AI808820 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK021957 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK126618 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL356796 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL445543 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AY149237 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC007696 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC035728 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC080610 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BU076480 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471090 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068269 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
MW752852 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
MW752853 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | ENST00000356083 ⟹ ENSP00000348385 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000451716 ⟹ ENSP00000391328 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000468565 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000477421 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000485397 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000490831 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000494090 ⟹ ENSP00000432928 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000494780 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | NM_032888 ⟹ NP_116277 | ||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | XM_006717308 ⟹ XP_006717371 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006717310 ⟹ XP_006717373 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011519138 ⟹ XP_011517440 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011519140 ⟹ XP_011517442 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011519142 ⟹ XP_011517444 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011519143 ⟹ XP_011517445 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011519144 ⟹ XP_011517446 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011519145 ⟹ XP_011517447 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017015239 ⟹ XP_016870728 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_047423992 ⟹ XP_047279948 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047423993 ⟹ XP_047279949 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047423994 ⟹ XP_047279950 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047423995 ⟹ XP_047279951 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364055 ⟹ XP_054220030 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364056 ⟹ XP_054220031 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364057 ⟹ XP_054220032 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364058 ⟹ XP_054220033 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364059 ⟹ XP_054220034 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364060 ⟹ XP_054220035 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364061 ⟹ XP_054220036 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364062 ⟹ XP_054220037 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364063 ⟹ XP_054220038 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364064 ⟹ XP_054220039 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364065 ⟹ XP_054220040 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364066 ⟹ XP_054220041 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054364067 ⟹ XP_054220042 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_008488095 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_929860 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
||||||||
Sequence: |
Protein RefSeqs | NP_116277 | (Get FASTA) | NCBI Sequence Viewer |
XP_006717371 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006717373 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011517440 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011517442 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011517444 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011517445 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011517446 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011517447 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016870728 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047279948 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047279949 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047279950 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047279951 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220030 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220031 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220032 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220033 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220034 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220035 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220036 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220037 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220038 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220039 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220040 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220041 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054220042 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAH80610 | (Get FASTA) | NCBI Sequence Viewer |
AAN41263 | (Get FASTA) | NCBI Sequence Viewer | |
BAB13947 | (Get FASTA) | NCBI Sequence Viewer | |
BAB47499 | (Get FASTA) | NCBI Sequence Viewer | |
EAW87411 | (Get FASTA) | NCBI Sequence Viewer | |
EAW87412 | (Get FASTA) | NCBI Sequence Viewer | |
EAW87413 | (Get FASTA) | NCBI Sequence Viewer | |
EAW87414 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000348385 | ||
ENSP00000348385.3 | |||
ENSP00000391328.1 | |||
ENSP00000432928.1 | |||
GenBank Protein | Q8IZC6 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_116277 ⟸ NM_032888 |
- Peptide Label: | preproprotein |
- UniProtKB: | Q66K43 (UniProtKB/Swiss-Prot), Q96JF7 (UniProtKB/Swiss-Prot), Q8IZC6 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | XP_006717371 ⟸ XM_006717308 |
- Peptide Label: | isoform X3 |
- Sequence: |
RefSeq Acc Id: | XP_006717373 ⟸ XM_006717310 |
- Peptide Label: | isoform X11 |
- Sequence: |
RefSeq Acc Id: | XP_011517440 ⟸ XM_011519138 |
- Peptide Label: | isoform X1 |
- Sequence: |
RefSeq Acc Id: | XP_011517444 ⟸ XM_011519142 |
- Peptide Label: | isoform X6 |
- Sequence: |
RefSeq Acc Id: | XP_011517445 ⟸ XM_011519143 |
- Peptide Label: | isoform X7 |
- Sequence: |
RefSeq Acc Id: | XP_011517446 ⟸ XM_011519144 |
- Peptide Label: | isoform X8 |
- Sequence: |
RefSeq Acc Id: | XP_011517442 ⟸ XM_011519140 |
- Peptide Label: | isoform X2 |
- Sequence: |
RefSeq Acc Id: | XP_011517447 ⟸ XM_011519145 |
- Peptide Label: | isoform X13 |
- Sequence: |
RefSeq Acc Id: | XP_016870728 ⟸ XM_017015239 |
- Peptide Label: | isoform X9 |
- Sequence: |
RefSeq Acc Id: | ENSP00000391328 ⟸ ENST00000451716 |
RefSeq Acc Id: | ENSP00000432928 ⟸ ENST00000494090 |
RefSeq Acc Id: | ENSP00000348385 ⟸ ENST00000356083 |
RefSeq Acc Id: | XP_047279948 ⟸ XM_047423992 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_047279949 ⟸ XM_047423993 |
- Peptide Label: | isoform X5 |
RefSeq Acc Id: | XP_047279950 ⟸ XM_047423994 |
- Peptide Label: | isoform X10 |
RefSeq Acc Id: | XP_047279951 ⟸ XM_047423995 |
- Peptide Label: | isoform X12 |
RefSeq Acc Id: | XP_054220030 ⟸ XM_054364055 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054220033 ⟸ XM_054364058 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_054220031 ⟸ XM_054364056 |
- Peptide Label: | isoform X2 |
RefSeq Acc Id: | XP_054220032 ⟸ XM_054364057 |
- Peptide Label: | isoform X3 |
RefSeq Acc Id: | XP_054220034 ⟸ XM_054364059 |
- Peptide Label: | isoform X5 |
RefSeq Acc Id: | XP_054220036 ⟸ XM_054364061 |
- Peptide Label: | isoform X7 |
RefSeq Acc Id: | XP_054220037 ⟸ XM_054364062 |
- Peptide Label: | isoform X8 |
RefSeq Acc Id: | XP_054220035 ⟸ XM_054364060 |
- Peptide Label: | isoform X6 |
RefSeq Acc Id: | XP_054220038 ⟸ XM_054364063 |
- Peptide Label: | isoform X9 |
RefSeq Acc Id: | XP_054220039 ⟸ XM_054364064 |
- Peptide Label: | isoform X10 |
RefSeq Acc Id: | XP_054220041 ⟸ XM_054364066 |
- Peptide Label: | isoform X12 |
RefSeq Acc Id: | XP_054220040 ⟸ XM_054364065 |
- Peptide Label: | isoform X11 |
RefSeq Acc Id: | XP_054220042 ⟸ XM_054364067 |
- Peptide Label: | isoform X13 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-Q8IZC6-F1-model_v2 | AlphaFold | Q8IZC6 | 1-1860 | view protein structure |
RGD ID: | 7215955 | ||||||||
Promoter ID: | EPDNEW_H13723 | ||||||||
Type: | initiation region | ||||||||
Name: | COL27A1_1 | ||||||||
Description: | collagen type XXVII alpha 1 chain | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H13724 | ||||||||
Experiment Methods: | Single-end sequencing.; Paired-end sequencing. | ||||||||
Position: |
|
RGD ID: | 7215959 | ||||||||
Promoter ID: | EPDNEW_H13724 | ||||||||
Type: | initiation region | ||||||||
Name: | COL27A1_2 | ||||||||
Description: | collagen type XXVII alpha 1 chain | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H13723 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
RGD ID: | 6807404 | ||||||||
Promoter ID: | HG_KWN:64628 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | CD4+TCell, HeLa_S3 | ||||||||
Transcripts: | ENST00000356083, ENST00000357257 | ||||||||
Position: |
|
RGD ID: | 6807399 | ||||||||
Promoter ID: | HG_KWN:64634 | ||||||||
Type: | Non-CpG | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | CD4+TCell | ||||||||
Transcripts: | OTTHUMT00000053765, OTTHUMT00000315896 | ||||||||
Position: |
|
Database | Acc Id | Source(s) |
AGR Gene | HGNC:22986 | AgrOrtholog |
COSMIC | COL27A1 | COSMIC |
Ensembl Genes | ENSG00000196739 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000356083 | ENTREZGENE |
ENST00000356083.8 | UniProtKB/Swiss-Prot | |
ENST00000451716.5 | UniProtKB/TrEMBL | |
ENST00000494090.6 | UniProtKB/TrEMBL | |
Gene3D-CATH | 2.60.120.1000 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
2.60.120.200 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
GTEx | ENSG00000196739 | GTEx |
HGNC ID | HGNC:22986 | ENTREZGENE |
Human Proteome Map | COL27A1 | Human Proteome Map |
InterPro | Collagen | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
ConA-like_dom_sf | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Fib_collagen_C | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
TSPN-like_N | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
KEGG Report | hsa:85301 | UniProtKB/Swiss-Prot |
NCBI Gene | 85301 | ENTREZGENE |
OMIM | 608461 | OMIM |
PANTHER | COLLAGEN | UniProtKB/TrEMBL |
COLLAGEN ALPHA | UniProtKB/Swiss-Prot | |
COLLAGEN ALPHA-1(XXVII) CHAIN | UniProtKB/Swiss-Prot | |
PTHR37456:SF5 | UniProtKB/TrEMBL | |
SI:CH211-266K2.1 | UniProtKB/TrEMBL | |
Pfam | COLFI | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Collagen | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
PharmGKB | PA134990818 | PharmGKB |
PRINTS | PRICHEXTENSN | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PROSITE | NC1_FIB | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
SMART | COLFI | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
TSPN | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Superfamily-SCOP | SSF49899 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
UniProt | CORA1_HUMAN | UniProtKB/Swiss-Prot |
H0YD40_HUMAN | UniProtKB/TrEMBL | |
Q5T1U7_HUMAN | UniProtKB/TrEMBL | |
Q66K43 | ENTREZGENE | |
Q8IZC6 | ENTREZGENE | |
Q96JF7 | ENTREZGENE | |
Q9HAA3_HUMAN | UniProtKB/TrEMBL | |
UniProt Secondary | Q66K43 | UniProtKB/Swiss-Prot |
Q96JF7 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2016-07-26 | COL27A1 | collagen type XXVII alpha 1 chain | COL27A1 | collagen type XXVII alpha 1 | Symbol and/or name change | 5135510 | APPROVED |
2016-01-26 | COL27A1 | collagen type XXVII alpha 1 | COL27A1 | collagen, type XXVII, alpha 1 | Symbol and/or name change | 5135510 | APPROVED |