Variant #0000529787 (NC_000005.9:g.143625_143626insG, NC_000005.9(NM_052909.3):c.743+7_743+8insG (PLEKHG4B))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.143625_143626insG
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PLEKHG4B_000054
Frequency 5/12514
Freq. EA 2/8248
Freq. AA 3/4266
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 22:05:22 +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+7_743+8insG r.(=) p.(=)