Variant #0000948181 (NC_000003.11:g.4732893C>T, NM_001168272.1:c.3849C>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.4732893C>T
DNA change (hg38) -
Published as ITPR1(NM_001168272.1):c.3849C>T (p.N1283=)
ISCN -
DB-ID ITPR1_000169
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) 0.00055 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +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     
ITPR1 NM_001168272.1 -?/. - c.3849C>T r.(?) p.(=)
ITPR1 NM_001378452.1 -?/. - c.3894C>T r.(?) p.(Asn1298=)


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