Variant #0001369387 (NC_000015.9:g.20644846C>T, NR_036432.1:n.3006G>A (HERC2P3))
Chromosome |
15 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.20644846C>T |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
HERC2P3_000027 |
Frequency |
1/8416 |
Freq. EA |
0/5398 |
Freq. AA |
1/3018 |
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 20:15:46 +02:00 (CEST) |

Variant on transcripts
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