Variant #0001055765 (NC_000017.10:g.1401231T>G, NM_001135642.1:c.734A>C (INPP5K))

Chromosome 17
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.1401231T>G
DNA change (hg38) -
Published as INPP5K(NM_016532.4):c.962A>C (p.(Glu321Ala))
ISCN -
DB-ID INPP5K_000016
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INPP5K NM_001135642.1 ?/. - c.734A>C r.(?) p.(Glu245Ala)
INPP5K NM_016532.3 ?/. - c.962A>C r.(?) p.(Glu321Ala)


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