Variant #0000111557 (NC_000001.10:g.147091689G>A, NM_004326.2:c.1728G>A (BCL9))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.147091689G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL9_000089
Frequency 357/13006
Freq. EA 333/8600
Freq. AA 24/4406
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 19:29:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL9 NM_004326.2 ?/? c.1728G>A r.(=) p.(=)