Variant #0000551262 (NC_000005.9:g.60199573T>C, NC_000005.9(NM_000082.3):c.482-30A>G (ERCC8))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.60199573T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC8_000065
Frequency 1/13002
Freq. EA 0/8598
Freq. AA 1/4404
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 06:42:05 +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.482-30A>G r.(=) p.(=)