Variant #0001785949 (NC_000019.9:g.47735818C>T, NC_000019.9(NM_014417.4):c.-1648G>A (BBC3))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.47735818C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BBC3_000011
Frequency 14/4566
Freq. EA 14/3182
Freq. AA 0/1384
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 01:59:40 +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.-1648G>A r.(=) p.(=)