Variant #0001651886 (NC_000018.9:g.210453T>C, NM_005151.3:c.1293T>C (USP14))
| Chromosome |
18 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.210453T>C |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
USP14_000082 |
| Frequency |
60/13002 |
| Freq. EA |
1/8596 |
| Freq. AA |
59/4406 |
| 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 16:45:07 +02:00 (CEST) |
| Date last edited |
2014-05-23 22:30:38 +02:00 (CEST) |

Variant on transcripts
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