Variant #0001369396 (NC_000015.9:g.20645775C>G, NR_036432.1:n.2895G>C (HERC2P3))
Chromosome |
15 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.20645775C>G |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
HERC2P3_000044 |
Frequency |
158/12928 |
Freq. EA |
128/8534 |
Freq. AA |
30/4394 |
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 16:41:46 +02:00 (CEST) |
Date last edited |
2014-04-28 03:35:54 +02:00 (CEST) |

Variant on transcripts
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