Variant #0001785942 (NC_000019.9:g.47725036G>A, NM_014417.4:c.*23C>T (BBC3))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.47725036G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BBC3_000004
Frequency 84/13004
Freq. EA 75/8598
Freq. AA 9/4406
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 16:45:39 +02:00 (CEST)
Date last edited 2013-05-06 01:59:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BBC3 NM_014417.4 ?/? c.*23C>T r.(=) p.(=)