Variant #0000347364 (NC_000013.10:g.20763397_20763410del, NM_004004.5:c.313_326del (GJB2))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.20763397_20763410del
DNA change (hg38) g.20189258_20189271del
Published as GJB2(NM_004004.6):c.313_326delAAGTTCATCAAGGG (p.K105Gfs*5)
ISCN -
DB-ID GJB2_000026 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GJB2 NM_004004.5 +/. - c.313_326del r.(?) p.(Lys105GlyfsTer5)


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