Variant #0001168316 (NC_000012.11:g.4665519T>C, NM_006479.4:c.722T>C (RAD51AP1))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.4665519T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RAD51AP1_000071
Frequency 7/13006
Freq. EA 0/8600
Freq. AA 7/4406
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 16:39:18 +02:00 (CEST)
Date last edited 2013-05-05 01:23:22 +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.722T>C r.(?) p.(Val241Ala)