Variant #0001063852 (NC_000003.11:g.4856104C>T, NC_000003.11(NM_001168272.1):c.7517-3C>T (ITPR1))

Chromosome 3
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.4856104C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ITPR1_000228
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.7517-3C>T r.spl? p.?
ITPR1 NM_001378452.1 -?/. - c.7562-3C>T r.spl? p.?


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