Variant #0000111499 (NC_000001.10:g.147087584G>C, NC_000001.10(NM_004326.2):c.561-19G>C (BCL9))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.147087584G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL9_000026
Frequency 7/13006
Freq. EA 0/8600
Freq. AA 7/4406
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 19:29:15 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL9 NM_004326.2 ?/? c.561-19G>C r.(=) p.(=)