Variant #0000529786 (NC_000005.9:g.143625C>T, NC_000005.9(NM_052909.3):c.743+7C>T (PLEKHG4B))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.143625C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PLEKHG4B_000053
Frequency 2/12998
Freq. EA 0/8594
Freq. AA 2/4404
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 2014-05-04 16:35:27 +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.743+7C>T r.(=) p.(=)