Variant #0000551296 (NC_000005.9:g.60234091G>A, NC_000005.9(NM_000082.3):c.77+6668C>T (ERCC8))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.60234091G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC8_000108
Frequency 3/4564
Freq. EA 0/3180
Freq. AA 3/1384
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 2013-05-04 06:42:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC8 NM_000082.3 ?/? c.77+6668C>T r.(=) p.(=)