Variant #0001465556 (NC_000016.9:g.14026007G>A, NC_000016.9(NM_005236.2):c.974-7G>A (ERCC4))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.14026007G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC4_000063
Frequency 12794/12994
Freq. EA 8419/8600
Freq. AA 4375/4394
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 16:42:42 +02:00 (CEST)
Date last edited 2013-05-05 12:42:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC4 NM_005236.2 ?/? c.974-7G>A r.(=) p.(=)