Variant #0000340255 (NC_000002.11:g.242509636T>C, NM_032515.4:c.446T>C (BOK))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.242509636T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BOK_000031
Frequency 1/12978
Freq. EA 1/8590
Freq. AA 0/4388
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 16:22:05 +02:00 (CEST)
Date last edited 2013-05-04 01:16:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BOK NM_032515.4 ?/? c.446T>C r.(?) p.(Leu149Pro)