Variant #0001578340 (NC_000017.10:g.33430313T>C, NM_002878.3:c.698A>G (RAD51D))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.33430313T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RAD51D_000028
Frequency 165/13006
Freq. EA 145/8600
Freq. AA 20/4406
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 2013-05-05 17:08:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RAD51D NM_002878.3 ?/? c.698A>G r.(?) p.(Glu233Gly)