Variant #0000454496 (NC_000004.11:g.85889T>C, NM_182524.2:c.494T>C (ZNF595))
Chromosome |
4 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.85889T>C |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
ZNF595_000016 |
Frequency |
4/12444 |
Freq. EA |
1/8394 |
Freq. AA |
3/4050 |
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 16:25:12 +02:00 (CEST) |
Date last edited |
2014-04-28 19:35:23 +02:00 (CEST) |

Variant on transcripts
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