Variant #0000529793 (NC_000005.9:g.144974T>C, NM_052909.3:c.776T>C (PLEKHG4B))
Chromosome |
5 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.144974T>C |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
PLEKHG4B_000060 |
Frequency |
5/13004 |
Freq. EA |
0/8598 |
Freq. AA |
5/4406 |
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 16:26:58 +02:00 (CEST) |
Date last edited |
2014-04-28 16:05:34 +02:00 (CEST) |

Variant on transcripts
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