Variant #0000988600 (NC_000010.10:g.50738781T>C, NM_000124.2:c.528A>G (ERCC6))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.50738781T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC6_000348
Frequency 88/13006
Freq. EA 80/8600
Freq. AA 8/4406
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 22:12:25 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC6 NM_000124.2 ?/? c.528A>G r.(=) p.(=)