Variant #0000975876 (NC_000003.11:g.4854831G>A, NM_001168272.1:c.7429G>A (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.4854831G>A
DNA change (hg38) -
Published as ITPR1(NM_001099952.2):c.7330G>A (p.(Gly2444Ser))
ISCN -
DB-ID ITPR1_000180
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) 3.0E-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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITPR1 NM_001168272.1 -?/. - c.7429G>A r.(?) p.(Gly2477Ser)
ITPR1 NM_001378452.1 -?/. - c.7474G>A r.(?) p.(Gly2492Ser)


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