Variant #0000529811 (NC_000005.9:g.155121C>A, NC_000005.9(NM_052909.3):c.1041+15C>A (PLEKHG4B))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.155121C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PLEKHG4B_000073
Frequency 32/13006
Freq. EA 1/8600
Freq. AA 31/4406
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 2014-03-27 13:45:13 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PLEKHG4B NM_052909.3 ?/? c.1041+15C>A r.(=) p.(=)