Variant #0001651879 (NC_000018.9:g.210044C>T, NC_000018.9(NM_005151.3):c.1225+13C>T (USP14))
Chromosome |
18 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.210044C>T |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
USP14_000076 |
Frequency |
59/13002 |
Freq. EA |
1/8596 |
Freq. AA |
58/4406 |
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 |
2014-04-28 11:50:41 +02:00 (CEST) |

Variant on transcripts
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