Variant #0000529782 (NC_000005.9:g.143534G>A, NM_052909.3:c.659G>A (PLEKHG4B))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.143534G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PLEKHG4B_000049
Frequency 2682/12994
Freq. EA 1064/8590
Freq. AA 1618/4404
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:26:58 +02:00 (CEST)
Date last edited 2014-05-03 22:05:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PLEKHG4B NM_052909.3 ?/? c.659G>A r.(?) p.(Arg220His)