Variant #0000809669 (NC_000008.10:g.190848G>T, NM_173539.2:c.-48G>T (ZNF596))
Chromosome |
8 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.190848G>T |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
ZNF596_000004 |
Frequency |
2/12008 |
Freq. EA |
0/8238 |
Freq. AA |
2/3770 |
Average frequency (gnomAD v.2.1.1) |
- |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Ivo F.A.C. Fokkema |
Date created |
2013-05-03 16:29:29 +02:00 (CEST) |
Date last edited |
2014-04-28 05:45:56 +02:00 (CEST) |

Variant on transcripts
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