Variant #0000111555 (NC_000001.10:g.147091663_147091665del, NM_004326.2:c.1702_1704del (BCL9))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.147091663_147091665del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL9_000087
Frequency 20/12520
Freq. EA 4/8254
Freq. AA 16/4266
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.1702_1704del r.(?) p.(Met568del)