C8orf37-AS1 (C8orf37 antisense RNA 1) - Rat Genome Database

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Gene: C8orf37-AS1 (C8orf37 antisense RNA 1) Homo sapiens
Analyze
Symbol: C8orf37-AS1
Name: C8orf37 antisense RNA 1
RGD ID: 8553073
HGNC Page HGNC
Description: ASSOCIATED WITH Bardet-Biedl Syndrome, 21; cone-rod dystrophy; cone-rod dystrophy 16; INTERACTS WITH aflatoxin B1; benzo[a]pyrene; O-methyleugenol
Type: ncrna
RefSeq Status: VALIDATED
Also known as: CFAP418-AS1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl895,204,456 - 95,811,254 (+)EnsemblGRCh38hg38GRCh38
GRCh38895,268,836 - 95,810,143 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37896,281,064 - 96,822,371 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8q22.1NCBI
HuRef891,488,509 - 92,028,475 (+)NCBIHuRef
CHM1_1896,321,316 - 96,862,765 (+)NCBICHM1_1
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
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
1. RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
Additional References at PubMed
PMID:23251661   PMID:23350875   PMID:23568457  


Genomics

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:440
Count of miRNA genes:374
Interacting mature miRNAs:394
Transcripts:ENST00000517437, ENST00000517655, ENST00000521905
Prediction methods:Miranda, Rnahybrid
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.


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 1 4 1
Low 31 12 41 22 183 19 37 9 74 127 385 113 5 1 3 13 1 1
Below cutoff 1649 1903 1244 364 983 236 3166 1298 3139 240 855 1234 142 822 2057 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NR_038201 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_038202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_038203 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_038204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_038205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_038206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_038207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_038208 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_038209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC024995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC083836 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC108924 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC116154 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295153 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295154 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295155 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295157 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295158 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295163 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GU295164 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458800 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458806 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459912 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459915 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459916 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459917 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459919 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000517437
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl895,432,637 - 95,810,136 (+)Ensembl
RefSeq Acc Id: ENST00000517655
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl895,204,456 - 95,432,666 (+)Ensembl
RefSeq Acc Id: ENST00000521905
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl895,268,836 - 95,653,710 (+)Ensembl
RefSeq Acc Id: ENST00000614093
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl895,798,395 - 95,800,649 (+)Ensembl
RefSeq Acc Id: ENST00000655917
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl895,268,835 - 95,802,821 (+)Ensembl
RefSeq Acc Id: ENST00000663556
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl895,800,578 - 95,811,079 (+)Ensembl
RefSeq Acc Id: ENST00000664790
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl895,610,664 - 95,811,254 (+)Ensembl
RefSeq Acc Id: ENST00000671532
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl895,268,823 - 95,802,733 (+)Ensembl
RefSeq Acc Id: NR_038201
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38895,268,836 - 95,810,143 (+)NCBI
HuRef891,488,509 - 92,028,475 (+)NCBI
CHM1_1896,321,316 - 96,862,765 (+)NCBI
Sequence:
RefSeq Acc Id: NR_038202
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38895,268,836 - 95,810,143 (+)NCBI
HuRef891,488,509 - 92,028,475 (+)NCBI
CHM1_1896,321,316 - 96,862,765 (+)NCBI
Sequence:
RefSeq Acc Id: NR_038203
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38895,268,836 - 95,810,143 (+)NCBI
HuRef891,488,509 - 92,028,475 (+)NCBI
CHM1_1896,321,316 - 96,862,765 (+)NCBI
Sequence:
RefSeq Acc Id: NR_038204
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38895,268,836 - 95,810,143 (+)NCBI
HuRef891,488,509 - 92,028,475 (+)NCBI
CHM1_1896,321,316 - 96,862,765 (+)NCBI
Sequence:
RefSeq Acc Id: NR_038205
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38895,268,836 - 95,810,143 (+)NCBI
HuRef891,488,509 - 92,028,475 (+)NCBI
CHM1_1896,321,316 - 96,862,765 (+)NCBI
Sequence:
RefSeq Acc Id: NR_038206
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38895,268,836 - 95,810,143 (+)NCBI
HuRef891,488,509 - 92,028,475 (+)NCBI
CHM1_1896,321,316 - 96,862,765 (+)NCBI
Sequence:
RefSeq Acc Id: NR_038207
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38895,268,836 - 95,810,143 (+)NCBI
HuRef891,488,509 - 92,028,475 (+)NCBI
CHM1_1896,321,316 - 96,862,765 (+)NCBI
Sequence:
RefSeq Acc Id: NR_038208
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38895,268,836 - 95,810,143 (+)NCBI
HuRef891,488,509 - 92,028,475 (+)NCBI
CHM1_1896,321,316 - 96,862,765 (+)NCBI
Sequence:
RefSeq Acc Id: NR_038209
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38895,268,836 - 95,810,143 (+)NCBI
HuRef891,488,509 - 92,028,475 (+)NCBI
CHM1_1896,321,316 - 96,862,765 (+)NCBI
Sequence:
Reference Sequences

Promoters
RGD ID:15096253
Promoter ID:EPDNEWNC_H1077
Type:multiple initiation site
Name:C8orf37-AS1_1
Description:C8orf37 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:50444]
SO ACC ID:SO:0000170
Source:EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38895,268,835 - 95,268,895EPDNEWNC

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_177965.4(C8orf37):c.155+2T>C single nucleotide variant Cone-rod dystrophy 16 [RCV000477722] Chr8:95269033 [GRCh38]
Chr8:96281261 [GRCh37]
Chr8:8q22.1
pathogenic
NR_038201.1(C8orf37-AS1):n.282-72416C>G single nucleotide variant Lung cancer [RCV000107901] Chr8:95538248 [GRCh38]
Chr8:96550476 [GRCh37]
Chr8:8q22.1
uncertain significance
NR_038201.1(C8orf37-AS1):n.316-32925A>G single nucleotide variant Lung cancer [RCV000107902] Chr8:95767571 [GRCh38]
Chr8:96779799 [GRCh37]
Chr8:8q22.1
uncertain significance
GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3 copy number gain See cases [RCV000134353] Chr8:94682154..145068656 [GRCh38]
Chr8:95694382..146294042 [GRCh37]
Chr8:95763558..146264846 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q21.3-24.23(chr8:86300584-137022587)x3 copy number gain See cases [RCV000135621] Chr8:86300584..137022587 [GRCh38]
Chr8:87312813..138034830 [GRCh37]
Chr8:87381929..138104012 [NCBI36]
Chr8:8q21.3-24.23
pathogenic|likely pathogenic
GRCh38/hg38 8q22.1(chr8:93038175-95667782)x1 copy number loss See cases [RCV000136519] Chr8:93038175..95667782 [GRCh38]
Chr8:94050403..96680010 [GRCh37]
Chr8:94119579..96749186 [NCBI36]
Chr8:8q22.1
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.3-24.3(chr8:87931152-145068712)x3 copy number gain See cases [RCV000138551] Chr8:87931152..145068712 [GRCh38]
Chr8:88943380..146294098 [GRCh37]
Chr8:89012496..146264902 [NCBI36]
Chr8:8q21.3-24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3 copy number gain See cases [RCV000139539] Chr8:46031340..139285494 [GRCh38]
Chr8:46942962..140297737 [GRCh37]
Chr8:47062127..140366919 [NCBI36]
Chr8:8q11.1-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.2-24.3(chr8:85765999-145070385)x3 copy number gain See cases [RCV000143659] Chr8:85765999..145070385 [GRCh38]
Chr8:86778228..146295771 [GRCh37]
Chr8:86863079..146266575 [NCBI36]
Chr8:8q21.2-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:95606052-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|See cases [RCV000053677] Chr8:95606052..145054775 [GRCh38]
Chr8:96618280..146280161 [GRCh37]
Chr8:96687456..146250965 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-22.1(chr8:78672463-95366868)x1 copy number loss See cases [RCV000054262] Chr8:78672463..95366868 [GRCh38]
Chr8:79584698..96379096 [GRCh37]
Chr8:79747253..96448272 [NCBI36]
Chr8:8q21.13-22.1
pathogenic
GRCh38/hg38 8q21.3-22.1(chr8:92283179-95786443)x1 copy number loss See cases [RCV000054265] Chr8:92283179..95786443 [GRCh38]
Chr8:93295407..96798671 [GRCh37]
Chr8:93364583..96867847 [NCBI36]
Chr8:8q21.3-22.1
pathogenic
GRCh38/hg38 8q21.3-22.1(chr8:92287062-95786443)x1 copy number loss See cases [RCV000054277] Chr8:92287062..95786443 [GRCh38]
Chr8:93299290..96798671 [GRCh37]
Chr8:93368466..96867847 [NCBI36]
Chr8:8q21.3-22.1
pathogenic
GRCh38/hg38 8q22.1(chr8:92755532-97792132)x1 copy number loss See cases [RCV000054278] Chr8:92755532..97792132 [GRCh38]
Chr8:93767760..98804360 [GRCh37]
Chr8:93836936..98873536 [NCBI36]
Chr8:8q22.1
pathogenic
NM_177965.4(C8orf37):c.55C>G (p.Pro19Ala) single nucleotide variant Cone-rod dystrophy 16 [RCV000296275]|Retinitis pigmentosa [RCV000388385]|none provided [RCV001282633]|not specified [RCV000730956] Chr8:95269135 [GRCh38]
Chr8:96281363 [GRCh37]
Chr8:8q22.1
benign|likely benign
NM_177965.3(C8orf37):c.-22G>A single nucleotide variant Cone-Rod Dystrophy, Recessive [RCV000338786]|Retinitis Pigmentosa, Recessive [RCV000281085] Chr8:95269211 [GRCh38]
Chr8:96281439 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.126G>C (p.Arg42=) single nucleotide variant Cone-rod dystrophy 16 [RCV001169701]|Retinitis pigmentosa [RCV001169700]|not provided [RCV000883271]|not specified [RCV000322042] Chr8:95269064 [GRCh38]
Chr8:96281292 [GRCh37]
Chr8:8q22.1
benign|uncertain significance
NM_177965.4(C8orf37):c.-5T>C single nucleotide variant Cone-rod dystrophy 16 [RCV000403058]|Retinitis pigmentosa [RCV000348812] Chr8:95269194 [GRCh38]
Chr8:96281422 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.17A>G (p.Asp6Gly) single nucleotide variant not provided [RCV001055608] Chr8:95269173 [GRCh38]
Chr8:96281401 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.155+8G>A single nucleotide variant Cone-rod dystrophy 16 [RCV001169699]|Retinitis pigmentosa [RCV001169698]|not provided [RCV000971378] Chr8:95269027 [GRCh38]
Chr8:96281255 [GRCh37]
Chr8:8q22.1
likely benign|uncertain significance
NM_177965.4(C8orf37):c.16_19del (p.Asp6fs) deletion C8orf37-Related Disorders [RCV000778138] Chr8:95269171..95269174 [GRCh38]
Chr8:96281399..96281402 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.15G>A (p.Leu5=) single nucleotide variant Cone-rod dystrophy 16 [RCV001165717]|Retinitis pigmentosa [RCV001165716] Chr8:95269175 [GRCh38]
Chr8:96281403 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.134C>G (p.Ala45Gly) single nucleotide variant not provided [RCV001226362] Chr8:95269056 [GRCh38]
Chr8:96281284 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.94G>A (p.Gly32Ser) single nucleotide variant Cone-rod dystrophy 16 [RCV000988098] Chr8:95269096 [GRCh38]
Chr8:96281324 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.130C>T (p.Gln44Ter) single nucleotide variant Bardet-Biedl syndrome 21 [RCV001000091] Chr8:95269060 [GRCh38]
Chr8:96281288 [GRCh37]
Chr8:8q22.1
likely pathogenic
NM_177965.4(C8orf37):c.16G>A (p.Asp6Asn) single nucleotide variant not provided [RCV001068065] Chr8:95269174 [GRCh38]
Chr8:96281402 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.88C>G (p.Pro30Ala) single nucleotide variant not provided [RCV001237005] Chr8:95269102 [GRCh38]
Chr8:96281330 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.118A>G (p.Ser40Gly) single nucleotide variant not provided [RCV001039130] Chr8:95269072 [GRCh38]
Chr8:96281300 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.74G>A (p.Gly25Asp) single nucleotide variant not provided [RCV001308532] Chr8:95269116 [GRCh38]
Chr8:96281344 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.26T>C (p.Leu9Ser) single nucleotide variant not provided [RCV001351999] Chr8:95269164 [GRCh38]
Chr8:96281392 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.155+12G>A single nucleotide variant not provided [RCV001349718] Chr8:95269023 [GRCh38]
Chr8:96281251 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.134C>T (p.Ala45Val) single nucleotide variant not provided [RCV001344323] Chr8:95269056 [GRCh38]
Chr8:96281284 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.55C>T (p.Pro19Ser) single nucleotide variant not provided [RCV001324612] Chr8:95269135 [GRCh38]
Chr8:96281363 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.71G>A (p.Arg24Gln) single nucleotide variant not provided [RCV001297195] Chr8:95269119 [GRCh38]
Chr8:96281347 [GRCh37]
Chr8:8q22.1
uncertain significance
NM_177965.4(C8orf37):c.43A>G (p.Lys15Glu) single nucleotide variant not provided [RCV001352243] Chr8:95269147 [GRCh38]
Chr8:96281375 [GRCh37]
Chr8:8q22.1
uncertain significance

Additional Information

Database Acc Id Source(s)
COSMIC C8orf37-AS1 COSMIC
Ensembl Genes ENSG00000253773 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000517437 ENTREZGENE
GTEx ENSG00000253773 GTEx
HGNC ID HGNC:50444 ENTREZGENE
Human Proteome Map C8orf37-AS1 Human Proteome Map
NCBI Gene C8orf37-AS1 ENTREZGENE
RNAcentral URS0000759AFC RNACentral
  URS0000759B10 RNACentral
  URS000075A4ED RNACentral
  URS000075B39B RNACentral
  URS000075B3DB RNACentral
  URS000075B725 RNACentral
  URS000075C262 RNACentral
  URS000075DBB3 RNACentral
  URS000075EC8E RNACentral