Variant #0000988548 (NC_000010.10:g.50725062A>T, NC_000010.10(NM_000124.2):c.1397+7017T>A (ERCC6))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.50725062A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC6_000350
Frequency 2/13006
Freq. EA 1/8600
Freq. AA 1/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:30:47 +02:00 (CEST)
Date last edited 2013-08-22 22:22:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC6 NM_000124.2 ?/? c.1397+7017T>A r.(=) p.(=)
PGBD3 NM_170753.2 ?/? c.99T>A r.(=) p.(=)