Variant #0000809692 (NC_000008.10:g.193699A>C, NC_000008.10(NM_173539.2):c.140-23A>C (ZNF596))
Chromosome |
8 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.193699A>C |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
ZNF596_000027 |
Frequency |
13/13006 |
Freq. EA |
0/8600 |
Freq. AA |
13/4406 |
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 16:05:29 +02:00 (CEST) |

Variant on transcripts
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