Variant #0001050737 (NC_000002.11:g.99155375A>G, NM_001134225.1:c.601A>G (INPP4A))

Chromosome 2
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.99155375A>G
DNA change (hg38) -
Published as INPP4A(NM_001134225.2):c.601A>G (p.(Ser201Gly))
ISCN -
DB-ID INPP4A_000012
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INPP4A NM_001134225.1 ?/. - c.601A>G r.(?) p.(Ser201Gly)
INPP4A NM_001566.2 ?/. - c.601A>G r.(?) p.(Ser201Gly)


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