COL27A1 (collagen type XXVII alpha 1 chain) - Rat Genome Database

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Gene: COL27A1 (collagen type XXVII alpha 1 chain) Homo sapiens
Analyze
Symbol: COL27A1
Name: collagen type XXVII alpha 1 chain
RGD ID: 1350673
HGNC Page HGNC:22986
Description: An extracellular matrix structural constituent conferring tensile strength. Predicted to be involved in several processes, including collagen fibril organization; endothelial cell morphogenesis; and notochord development. Predicted to act upstream of or within extracellular matrix organization and growth plate cartilage chondrocyte development. Located in collagen-containing extracellular matrix.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: collagen alpha-1(XXVII) chain; collagen type XXVII alpha 1; collagen, type XXVII, alpha 1; FLJ11895; KIAA1870; MGC11337; RP11-82I1.1; STLS
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389114,154,098 - 114,312,511 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9114,155,537 - 114,312,511 (+)EnsemblGRCh38hg38GRCh38
GRCh379116,917,817 - 117,074,791 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 369115,958,052 - 116,112,796 (+)NCBINCBI36Build 36hg18NCBI36
Build 349113,997,784 - 114,152,529NCBI
Celera987,566,107 - 87,720,603 (+)NCBICelera
Cytogenetic Map9q32NCBI
HuRef986,524,630 - 86,679,150 (+)NCBIHuRef
CHM1_19117,064,706 - 117,219,685 (+)NCBICHM1_1
T2T-CHM13v2.09126,352,719 - 126,511,655 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,1-dichloroethene  (ISO)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (EXP,ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2-palmitoylglycerol  (EXP)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3,4-methylenedioxymethamphetamine  (ISO)
3-chloropropane-1,2-diol  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxyphenyl retinamide  (ISO)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
acrylamide  (ISO)
aflatoxin B1  (EXP)
aldehydo-D-glucose  (ISO)
aldrin  (ISO)
all-trans-retinoic acid  (EXP)
allethrin  (ISO)
amiodarone  (EXP)
ammonium chloride  (ISO)
amphetamine  (ISO)
antirheumatic drug  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
benzo[a]pyrene  (ISO)
beta-naphthoflavone  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
CGP 52608  (EXP)
choline  (ISO)
copper(II) sulfate  (EXP)
Cuprizon  (ISO)
curcumin  (ISO)
cyclosporin A  (EXP)
cyhalothrin  (ISO)
cypermethrin  (ISO)
D-glucose  (ISO)
dibutyl phthalate  (ISO)
dichloroacetic acid  (ISO)
dicrotophos  (EXP)
disodium selenite  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
ethanol  (ISO)
fenvalerate  (ISO)
folic acid  (ISO)
fructose  (ISO)
fulvestrant  (EXP)
glucose  (ISO)
glycidol  (ISO)
L-methionine  (ISO)
leflunomide  (ISO)
N-methyl-4-phenylpyridinium  (ISO)
N-nitrosodiethylamine  (ISO)
Nor-9-carboxy-delta9-THC  (EXP)
paracetamol  (EXP,ISO)
pentachlorophenol  (ISO)
perfluorooctane-1-sulfonic acid  (EXP)
phenobarbital  (ISO)
pirinixic acid  (ISO)
pyrethrins  (ISO)
resveratrol  (EXP)
SB 431542  (EXP)
sodium dichromate  (ISO)
sunitinib  (EXP)
tetrachloroethene  (ISO)
tetraphene  (ISO)
thioacetamide  (ISO)
trichostatin A  (EXP)
trimellitic anhydride  (ISO)
tris(2-butoxyethyl) phosphate  (EXP)
troglitazone  (ISO)
urethane  (EXP)
valproic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# 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
Additional References at PubMed
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  


Genomics

Comparative Map Data
COL27A1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389114,154,098 - 114,312,511 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9114,155,537 - 114,312,511 (+)EnsemblGRCh38hg38GRCh38
GRCh379116,917,817 - 117,074,791 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 369115,958,052 - 116,112,796 (+)NCBINCBI36Build 36hg18NCBI36
Build 349113,997,784 - 114,152,529NCBI
Celera987,566,107 - 87,720,603 (+)NCBICelera
Cytogenetic Map9q32NCBI
HuRef986,524,630 - 86,679,150 (+)NCBIHuRef
CHM1_19117,064,706 - 117,219,685 (+)NCBICHM1_1
T2T-CHM13v2.09126,352,719 - 126,511,655 (+)NCBIT2T-CHM13v2.0
Col27a1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39463,132,246 - 63,253,228 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl463,132,241 - 63,253,228 (+)EnsemblGRCm39 Ensembl
GRCm38463,214,009 - 63,334,991 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl463,214,004 - 63,334,991 (+)EnsemblGRCm38mm10GRCm38
MGSCv37462,876,446 - 62,996,025 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36462,702,187 - 62,819,669 (+)NCBIMGSCv36mm8
Celera461,872,330 - 61,991,872 (+)NCBICelera
Cytogenetic Map4B3NCBI
cM Map433.96NCBI
Col27a1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8581,662,822 - 81,781,502 (+)NCBIGRCr8
mRatBN7.2576,647,302 - 76,765,989 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl576,647,429 - 76,765,174 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx579,046,962 - 79,163,379 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0580,864,094 - 80,980,524 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0580,839,597 - 80,956,018 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0579,054,004 - 79,172,442 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl579,055,521 - 79,170,765 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0583,168,893 - 83,286,676 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4580,198,078 - 80,316,354 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1580,203,190 - 80,321,467 (+)NCBI
Celera575,584,269 - 75,698,202 (+)NCBICelera
Cytogenetic Map5q24NCBI
Col27a1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495541913,289,006 - 13,411,118 (-)NCBIChiLan1.0ChiLan1.0
COL27A1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21125,064,772 - 25,221,614 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1925,067,145 - 25,223,942 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0985,252,277 - 85,410,714 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.19113,619,322 - 113,777,099 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl9113,627,633 - 113,775,284 (+)Ensemblpanpan1.1panPan2
COL27A1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11168,413,101 - 68,548,408 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1168,420,263 - 68,546,947 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1166,815,437 - 66,950,500 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01169,536,838 - 69,671,970 (+)NCBIROS_Cfam_1.0
UMICH_Zoey_3.11168,052,533 - 68,187,417 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01168,083,568 - 68,228,679 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01168,822,715 - 68,957,841 (+)NCBIUU_Cfam_GSD_1.0
Col27a1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947183,711,795 - 183,833,263 (+)NCBIHiC_Itri_2
SpeTri2.0NW_0049364873,487,776 - 3,601,779 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
COL27A1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1254,770,093 - 254,923,823 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11254,768,576 - 254,924,893 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21285,841,755 - 285,901,568 (+)NCBISscrofa10.2Sscrofa10.2susScr3
COL27A1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11225,272,617 - 25,431,308 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1225,272,609 - 25,429,086 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603517,388,410 - 17,548,127 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Col27a1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462476020,861,505 - 20,979,826 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in COL27A1
2043 total Variants

Clinical 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
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4138
Count of miRNA genes:1156
Interacting mature miRNAs:1490
Transcripts:ENST00000356083, ENST00000451716, ENST00000468565, ENST00000477421, ENST00000485397, ENST00000490831, ENST00000494090, ENST00000494780
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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.

Markers in Region
SHGC-80791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379116,977,617 - 116,977,912UniSTSGRCh37
Build 369116,017,438 - 116,017,733RGDNCBI36
Celera987,625,532 - 87,625,827RGD
Cytogenetic Map9q32UniSTS
HuRef986,584,139 - 86,584,434UniSTS
TNG Radiation Hybrid Map942830.0UniSTS
SHGC-144392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379116,999,391 - 116,999,676UniSTSGRCh37
Build 369116,039,212 - 116,039,497RGDNCBI36
Celera987,647,308 - 87,647,593RGD
Cytogenetic Map9q32UniSTS
HuRef986,606,057 - 86,606,342UniSTS
TNG Radiation Hybrid Map942816.0UniSTS
SHGC-144544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379117,011,161 - 117,011,482UniSTSGRCh37
Build 369116,050,982 - 116,051,303RGDNCBI36
Celera987,659,078 - 87,659,399RGD
Cytogenetic Map9q32UniSTS
HuRef986,617,827 - 86,618,148UniSTS
TNG Radiation Hybrid Map942807.0UniSTS
SHGC-145671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379117,049,688 - 117,050,003UniSTSGRCh37
Build 369116,089,509 - 116,089,824RGDNCBI36
Celera987,697,319 - 87,697,634RGD
Cytogenetic Map9q32UniSTS
HuRef986,655,867 - 86,656,182UniSTS
TNG Radiation Hybrid Map942855.0UniSTS
SHGC-145701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379116,989,255 - 116,989,540UniSTSGRCh37
Build 369116,029,076 - 116,029,361RGDNCBI36
Celera987,637,169 - 87,637,454RGD
Cytogenetic Map9q32UniSTS
HuRef986,595,784 - 86,596,069UniSTS
TNG Radiation Hybrid Map942757.0UniSTS
SHGC-147982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379116,994,721 - 116,995,045UniSTSGRCh37
Build 369116,034,542 - 116,034,866RGDNCBI36
Celera987,642,636 - 87,642,960RGD
Cytogenetic Map9q32UniSTS
HuRef986,601,386 - 86,601,710UniSTS
TNG Radiation Hybrid Map942777.0UniSTS
WI-22523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379117,073,550 - 117,073,801UniSTSGRCh37
Build 369116,113,371 - 116,113,622RGDNCBI36
Celera987,721,178 - 87,721,430RGD
Cytogenetic Map9q32UniSTS
HuRef986,679,725 - 86,679,977UniSTS
GeneMap99-GB4 RH Map9357.94UniSTS
Whitehead-RH Map9429.0UniSTS
NCBI RH Map91004.2UniSTS
SHGC-153772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379117,072,637 - 117,072,914UniSTSGRCh37
Build 369116,112,458 - 116,112,735RGDNCBI36
Celera987,720,265 - 87,720,542RGD
Cytogenetic Map9q32UniSTS
HuRef986,678,812 - 86,679,089UniSTS
TNG Radiation Hybrid Map942870.0UniSTS
SHGC-156158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379117,023,145 - 117,023,481UniSTSGRCh37
Build 369116,062,966 - 116,063,302RGDNCBI36
Celera987,671,061 - 87,671,397RGD
Cytogenetic Map9q32UniSTS
HuRef986,629,810 - 86,630,146UniSTS
TNG Radiation Hybrid Map942844.0UniSTS
SHGC-8827  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379116,993,784 - 116,993,936UniSTSGRCh37
Build 369116,033,605 - 116,033,757RGDNCBI36
Celera987,641,699 - 87,641,851RGD
Cytogenetic Map9q32UniSTS
HuRef986,600,449 - 86,600,601UniSTS
Stanford-G3 RH Map93896.0UniSTS
D1S1361  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p21.1-p12.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map17q21UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

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

Sequence

Nucleotide Sequences
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:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9114,155,537 - 114,312,511 (+)Ensembl
RefSeq Acc Id: ENST00000451716   ⟹   ENSP00000391328
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9114,167,715 - 114,218,579 (+)Ensembl
RefSeq Acc Id: ENST00000468565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9114,307,032 - 114,311,528 (+)Ensembl
RefSeq Acc Id: ENST00000477421
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9114,268,807 - 114,274,230 (+)Ensembl
RefSeq Acc Id: ENST00000485397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9114,240,220 - 114,246,121 (+)Ensembl
RefSeq Acc Id: ENST00000490831
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9114,306,213 - 114,309,339 (+)Ensembl
RefSeq Acc Id: ENST00000494090   ⟹   ENSP00000432928
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9114,168,608 - 114,311,548 (+)Ensembl
RefSeq Acc Id: ENST00000494780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9114,300,362 - 114,301,542 (+)Ensembl
RefSeq Acc Id: NM_032888   ⟹   NP_116277
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,312,511 (+)NCBI
GRCh379116,918,231 - 117,072,975 (+)RGD
Build 369115,958,052 - 116,112,796 (+)NCBI Archive
Celera987,566,107 - 87,720,603 (+)RGD
HuRef986,524,630 - 86,679,150 (+)ENTREZGENE
CHM1_19117,064,300 - 117,221,507 (+)NCBI
T2T-CHM13v2.09126,354,203 - 126,511,655 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006717308   ⟹   XP_006717371
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,312,511 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006717310   ⟹   XP_006717373
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,206,251 - 114,312,511 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011519138   ⟹   XP_011517440
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,154,098 - 114,312,511 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011519140   ⟹   XP_011517442
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,312,511 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011519142   ⟹   XP_011517444
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,284,315 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011519143   ⟹   XP_011517445
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,288,446 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011519144   ⟹   XP_011517446
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,288,446 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011519145   ⟹   XP_011517447
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,222,817 - 114,312,511 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017015239   ⟹   XP_016870728
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,275,748 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047423992   ⟹   XP_047279948
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,154,098 - 114,312,511 (+)NCBI
RefSeq Acc Id: XM_047423993   ⟹   XP_047279949
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,292,210 (+)NCBI
RefSeq Acc Id: XM_047423994   ⟹   XP_047279950
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,265,481 (+)NCBI
RefSeq Acc Id: XM_047423995   ⟹   XP_047279951
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,265,481 (+)NCBI
RefSeq Acc Id: XM_054364055   ⟹   XP_054220030
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,352,719 - 126,511,655 (+)NCBI
RefSeq Acc Id: XM_054364056   ⟹   XP_054220031
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,354,203 - 126,511,655 (+)NCBI
RefSeq Acc Id: XM_054364057   ⟹   XP_054220032
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,354,203 - 126,511,655 (+)NCBI
RefSeq Acc Id: XM_054364058   ⟹   XP_054220033
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,352,719 - 126,511,655 (+)NCBI
RefSeq Acc Id: XM_054364059   ⟹   XP_054220034
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,354,203 - 126,491,361 (+)NCBI
RefSeq Acc Id: XM_054364060   ⟹   XP_054220035
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,354,203 - 126,483,466 (+)NCBI
RefSeq Acc Id: XM_054364061   ⟹   XP_054220036
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,354,203 - 126,487,597 (+)NCBI
RefSeq Acc Id: XM_054364062   ⟹   XP_054220037
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,354,203 - 126,487,597 (+)NCBI
RefSeq Acc Id: XM_054364063   ⟹   XP_054220038
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,354,203 - 126,474,487 (+)NCBI
RefSeq Acc Id: XM_054364064   ⟹   XP_054220039
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,354,203 - 126,464,216 (+)NCBI
RefSeq Acc Id: XM_054364065   ⟹   XP_054220040
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,404,971 - 126,511,655 (+)NCBI
RefSeq Acc Id: XM_054364066   ⟹   XP_054220041
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,354,203 - 126,464,216 (+)NCBI
RefSeq Acc Id: XM_054364067   ⟹   XP_054220042
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,421,537 - 126,511,655 (+)NCBI
RefSeq Acc Id: XR_008488095
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.09126,354,203 - 126,505,698 (+)NCBI
RefSeq Acc Id: XR_929860
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,306,553 (+)NCBI
Sequence:
Protein Sequences
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
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8IZC6-F1-model_v2 AlphaFold Q8IZC6 1-1860 view protein structure

Promoters
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:
Human AssemblyChrPosition (strand)Source
GRCh389114,155,537 - 114,155,597EPDNEW
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:
Human AssemblyChrPosition (strand)Source
GRCh389114,168,583 - 114,168,643EPDNEW
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:
Human AssemblyChrPosition (strand)Source
Build 369115,957,329 - 115,957,829 (+)MPROMDB
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:
Human AssemblyChrPosition (strand)Source
Build 369116,107,906 - 116,108,406 (+)MPROMDB

Additional Information

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


Nomenclature History
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