Variant #0001164028 (NC_000012.11:g.266266T>C, NM_001170738.1:c.2229T>C (IQSEC3))
Chromosome |
12 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.266266T>C |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
IQSEC3_000080 |
Frequency |
779/13000 |
Freq. EA |
73/8596 |
Freq. AA |
706/4404 |
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 16:39:18 +02:00 (CEST) |
Date last edited |
2014-04-28 02:55:26 +02:00 (CEST) |

Variant on transcripts
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