Variant #0001168293 (NC_000012.11:g.4657293A>G, NM_006479.4:c.355A>G (RAD51AP1))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.4657293A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RAD51AP1_000048
Frequency 49/12998
Freq. EA 47/8596
Freq. AA 2/4402
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 16:39:18 +02:00 (CEST)
Date last edited 2013-05-05 01:23:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RAD51AP1 NM_006479.4 ?/? c.355A>G r.(?) p.(Met119Val)