Variant #0000071792 (NC_000013.10:g.20797467G>A, NM_006783.4:c.153C>T (GJB6))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.20797467G>A
DNA change (hg38) g.20223328G>A
Published as -
ISCN -
DB-ID GJB6_000019
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs185764408
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 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 09:47:00 +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.153C>T r.(=) p.(Phe51=)


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