Variant #0001785941 (NC_000019.9:g.47724914_47724917del, NM_014417.4:c.*142_*145del (BBC3))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.47724914_47724917del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BBC3_000003
Frequency 1247/7154
Freq. EA 823/4970
Freq. AA 424/2184
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.*142_*145del r.(=) p.(=)