Variant #0001909978 (NC_000022.10:g.23524466G>T, NC_000022.10(NM_004327.3):c.1279+40G>T (BCR))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.23524466G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCR_000055
Frequency 52/11640
Freq. EA 1/7706
Freq. AA 51/3934
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+40G>T r.(=) p.(=)