Variant #0000384655 (NC_000003.11:g.52438518A>C, NM_004656.2:c.1201T>G (BAP1))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.52438518A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BAP1_000070
Frequency 2/13006
Freq. EA 1/8600
Freq. AA 1/4406
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 16:23:53 +02:00 (CEST)
Date last edited 2013-05-04 02:21:50 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BAP1 NM_004656.2 ?/? c.1201T>G r.(?) p.(Tyr401Asp)