Variant #0001295499 (NC_000013.10:g.103513972G>A, NM_000123.3:c.788G>A (ERCC5))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.103513972G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ERCC5_000058
Frequency 5/13006
Freq. EA 5/8600
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 16:41:01 +02:00 (CEST)
Date last edited 2013-05-05 06:21:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ERCC5 NM_000123.3 ?/? c.788G>A r.(?) p.(Arg263Gln)