Variant #0001035099 (NC_000005.9:g.174108A>C, NM_052909.3:c.3229A>C (PLEKHG4B))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.174108A>C
DNA change (hg38) -
Published as PLEKHG4B(NM_052909.5):c.4297A>C (p.(Lys1433Gln))
ISCN -
DB-ID PLEKHG4B_000011
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEKHG4B NM_052909.3 ?/. - c.3229A>C r.(?) p.(Lys1077Gln)


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