Variant #0000447789 (NC_000003.11:g.187447625T>C, NM_001130845.1:c.568A>G (BCL6))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.187447625T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL6_000080
Frequency 2/13006
Freq. EA 2/8600
Freq. AA 0/4406
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 16:23:53 +02:00 (CEST)
Date last edited 2013-05-04 04:00:27 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL6 NM_001130845.1 ?/? c.568A>G r.(?) p.(Thr190Ala)