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 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:26:58 +02:00 (CEST)
Date last edited 2014-04-28 16:05:34 +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.776T>C r.(?) p.(Leu259Pro)