Variant #0001948321 (NC_000023.10:g.207362C>T, NM_018390.3:c.312C>T (PLCXD1))
| Chromosome |
X |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.207362C>T |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
PLCXD1_000044 |
| Frequency |
6655/12998 |
| Freq. EA |
5047/8592 |
| Freq. AA |
1608/4406 |
| 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 16:50:35 +02:00 (CEST) |
| Date last edited |
2014-05-03 19:50:26 +02:00 (CEST) |

Variant on transcripts
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