Variant #0001948328 (NC_000023.10:g.207451C>T, NC_000023.10(NM_018390.3):c.393+8C>T (PLCXD1))
Chromosome |
X |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.207451C>T |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
PLCXD1_000051 |
Frequency |
6180/12996 |
Freq. EA |
2646/8590 |
Freq. AA |
3534/4406 |
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 |
2014-05-20 00:10:22 +02:00 (CEST) |

Variant on transcripts
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