Variant #0001033543 (NC_000002.11:g.99172276G>A, NC_000002.11(NM_001134225.1):c.1822+5G>A (INPP4A))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.99172276G>A
DNA change (hg38) -
Published as INPP4A(NM_001134225.2):c.1822+5G>A
ISCN -
DB-ID INPP4A_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) 5.0E-5 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     
INPP4A NM_001134225.1 -?/. - c.1822+5G>A r.spl? p.?
INPP4A NM_001566.2 -?/. - c.1720+122G>A r.(=) p.(=)


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