Variant #0000551298 (NC_000005.9:g.60235194T>G, NC_000005.9(NM_000082.3):c.77+5565A>C (ERCC8))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.60235194T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC8_000112
Frequency 4/4566
Freq. EA 4/3182
Freq. AA 0/1384
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 16:26:58 +02:00 (CEST)
Date last edited 2013-08-22 18:08:27 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC8 NM_000082.3 ?/? c.77+5565A>C r.(=) p.(=)