Variant #0000988547 (NC_000010.10:g.50725028C>G, NC_000010.10(NM_000124.2):c.1397+7051G>C (ERCC6))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.50725028C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC6_000263
Frequency 2/13006
Freq. EA 2/8600
Freq. AA 0/4406
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 2013-05-04 19:21:21 +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+7051G>C r.(?) p.(Glu45Gln)
PGBD3 NM_170753.2 ?/? c.133G>C r.(?) p.(Glu45Gln)