Variant #0001613240 (NC_000017.10:g.56798128A>G, NM_058216.1:c.859A>G (RAD51C))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.56798128A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RAD51C_000051
Frequency 102/13006
Freq. EA 88/8600
Freq. AA 14/4406
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 16:44:12 +02:00 (CEST)
Date last edited 2016-07-30 22:34:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RAD51C NM_058216.1 ?/? c.859A>G r.(?) p.(Thr287Ala)