Variant #0000749184 (NC_000007.13:g.72971768G>A, NC_000007.13(NM_001707.3):c.92+49C>T (BCL7B))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.72971768G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL7B_000038
Frequency 4/12814
Freq. EA 3/8490
Freq. AA 1/4324
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 16:28:58 +02:00 (CEST)
Date last edited 2013-05-04 12:15:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL7B NM_001707.3 ?/? c.92+49C>T r.(=) p.(=)