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 International |
| 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) |

Variant on transcripts
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