Variant #0000749158 (NC_000007.13:g.72954163_72954164insA, NC_000007.13(NM_001707.3):c.436+48_436+49insT (BCL7B))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.72954163_72954164insA
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL7B_000012
Frequency 1/12516
Freq. EA 1/8254
Freq. AA 0/4262
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 12:15:44 +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.436+48_436+49insT r.(=) p.(=)