Variant #0000384698 (NC_000003.11:g.52440985G>A, NC_000003.11(NM_004656.2):c.581-62C>T (BAP1))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.52440985G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BAP1_000113
Frequency 1/4566
Freq. EA 0/3182
Freq. AA 1/1384
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 16:23:53 +02:00 (CEST)
Date last edited 2013-05-04 02:21:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BAP1 NM_004656.2 ?/? c.581-62C>T r.(=) p.(=)