Variant #0000809690 (NC_000008.10:g.193681G>T, NC_000008.10(NM_173539.2):c.140-41G>T (ZNF596))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.193681G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZNF596_000025
Frequency 3/13006
Freq. EA 0/8600
Freq. AA 3/4406
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 16:29:29 +02:00 (CEST)
Date last edited 2014-05-22 00:25:24 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZNF596 NM_173539.2 ?/? c.140-41G>T r.(=) p.(=)