Variant #0001063847 (NC_000003.11:g.4735396G>T, NM_001168272.1:c.4207G>T (ITPR1))

Chromosome 3
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.4735396G>T
DNA change (hg38) -
Published as ITPR1(NM_001378452.1):c.4252G>T (p.(Val1418Leu))
ISCN -
DB-ID ITPR1_000224
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITPR1 NM_001168272.1 ?/. - c.4207G>T r.(?) p.(Val1403Leu)
ITPR1 NM_001378452.1 ?/. - c.4252G>T r.(?) p.(Val1418Leu)


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