Variant #0000071791 (NC_000013.10:g.20797144T>C, NM_006783.4:c.476A>G (GJB6))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.20797144T>C
DNA change (hg38) g.20223005T>C
Published as -
ISCN -
DB-ID GJB6_000018
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs35277762
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00052 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-06-19 09:43:09 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GJB6 NM_006783.4 ?/? 3 c.476A>G r.(?) p.(Asn159Ser)


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