Variant #0001909979 (NC_000022.10:g.23540414T>G, NC_000022.10(NM_004327.3):c.1279+15988T>G (BCR))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.23540414T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCR_000056
Frequency 1641/5734
Freq. EA 1053/3982
Freq. AA 588/1752
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 16:50:05 +02:00 (CEST)
Date last edited 2013-05-06 07:28:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCR NM_004327.3 ?/? c.1279+15988T>G r.(=) p.(=)