Variant #0001948333 (NC_000023.10:g.207492G>A, NC_000023.10(NM_018390.3):c.393+49G>A (PLCXD1))
Chromosome |
X |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.207492G>A |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
PLCXD1_000056 |
Frequency |
5/12994 |
Freq. EA |
3/8590 |
Freq. AA |
2/4404 |
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 |
2014-06-20 06:16:54 +02:00 (CEST) |

Variant on transcripts
|
|