Variant #0003520714 (NC_000005.9:g.140532T>C, NM_052909.3:c.110T>C (PLEKHG4B))

Chromosome 5
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.140532T>C
DB-ID -
dbSNP ID rs12516846
gnomAD frequency 17749/158120
gnomAD homozygote count 1462/62773
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PLEKHG4B NM_052909.3 ./. c.110T>C r.(?) p.(Val37Ala)