Variant #0000809677 (NC_000008.10:g.190988T>C, NC_000008.10(NM_173539.2):c.12+81T>C (ZNF596))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.190988T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF596_000012
Frequency 6/4566
Freq. EA 0/3182
Freq. AA 6/1384
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 16:29:29 +02:00 (CEST)
Date last edited 2014-05-04 14:40:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF596 NM_173539.2 ?/? c.12+81T>C r.(=) p.(=)