chr13:20189451:C>G Detail (hg38) (GJB2)

Information

Genome

Assembly Position
hg19 chr13:20,763,590-20,763,590 View the variant detail on this assembly version.
hg38 chr13:20,189,451-20,189,451

HGVS

Type Transcript Protein
RefSeq NM_004004.5:c.131G>C NP_003995.2:p.Trp44Ser
Ensemble ENST00000382844.2:c.131G>C ENST00000382844.2:p.Trp44Ser
ENST00000382848.5:c.131G>C ENST00000382848.5:p.Trp44Ser
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 121011 OMIM
HGNC 4284 HGNC
Ensembl ENSG00000165474 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2003-04-15 no assertion criteria provided Autosomal dominant nonsyndromic hearing loss 3A germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.440 DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder) NA CLINVAR Detail
0.360 DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder) NA CLINVAR Detail
0.133 palmoplantar keratosis HeLa cells stably expressing nine dominant Cx26 mutants, six associated with non... BeFree 20096356 Detail
<0.001 palmoplantar keratosis HeLa cells stably expressing nine dominant Cx26 mutants, six associated with non... BeFree 20096356 Detail
0.133 palmoplantar keratosis HeLa cells stably expressing wild type Cx26 were transiently transfected to co-e... BeFree 21040787 Detail
0.012 Dermatologic disorders Here we compare the properties of four cx26 mutants derived from point mutations... BeFree 12668604 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_004004.6(GJB2):c.131G>C (p.Trp44Ser) AND Autosomal dominant nonsyndromic hearing loss 3A ClinVar Detail
NA DisGeNET Detail
NA DisGeNET Detail
HeLa cells stably expressing nine dominant Cx26 mutants, six associated with non-syndromic hearing l... DisGeNET Detail
HeLa cells stably expressing nine dominant Cx26 mutants, six associated with non-syndromic hearing l... DisGeNET Detail
HeLa cells stably expressing wild type Cx26 were transiently transfected to co-express nine individu... DisGeNET Detail
Here we compare the properties of four cx26 mutants derived from point mutations associated with dom... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs104894413 dbSNP
Genome
hg38
Position
chr13:20,189,451-20,189,451
Variant Type
snv
Reference Allele
C
Alternative Allele
G
Genome browser