Variant #0001214167 (NC_000012.11:g.56749163G>A, NC_000012.11(NM_005419.3):c.472-28C>T (STAT2))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.56749163G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID STAT2_000114
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 16:39:18 +02:00 (CEST)
Date last edited 2016-08-27 09:44:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
STAT2 NM_005419.3 ?/? c.472-28C>T r.(=) p.(=)