Overview

Variant ID 22519
Entrez Gene ID 6262
Gene RYR2 (GeneCards)
Location hg19 1:237274033-237274033
hg38 1:237110733-237110733
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000001.10:g.237274033 C>A (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 249250621

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.0322
CADD Raw score (version 1.3) 0.272885 (Deleterious)
FATHMM raw prediction score 0.15612 (Tolerated)
Deleterious probability by DeFine 0.5967 (Deleterious)
Entrez Gene ID 6262 (NCBI Gene)
Official Gene Symbol RYR2 (GeneCards)
Number of variants in RYR2 in this database 13 (view all the variants)
Full name ryanodine receptor 2
Band 1q43
Other IDs Vega: OTTHUMG00000039543
OMIM: 180902
HGNC: HGNC:10484
Ensembl: ENSG00000198626
Other names RyR, ARVC2, ARVD2, RYR-2, VTSIP
Summary This gene encodes a ryanodine receptor found in cardiac muscle sarcoplasmic reticulum. The encoded protein is one of the components of a calcium channel, composed of a tetramer of the ryanodine receptor proteins and a tetramer of FK506 binding protein 1B proteins, that supplies calcium to cardiac muscle. Mutations in this gene are associated with stress-induced polymorphic ventricular tachycardia and arrhythmogenic right ventricular dysplasia. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217587.01 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217587

Pubmed ID 29217587
Title Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis.
Journal Science
Publication date 2018.02
Disease Asymptomatic
Number of cases cases of unknown sex: 3;