Variant #0001794469 (NC_000019.9:g.50169081A>G, NM_001571.5:c.-202T>C (IRF3))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.50169081A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2L12_000001
Frequency 3/13000
Freq. EA 0/8596
Freq. AA 3/4404
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 02:23:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L12 NM_001040668.1 ?/? c.1A>G r.? p.?
IRF3 NM_001571.5 ?/? c.-202T>C r.? p.?