Variant ID | 22519 |
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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) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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) |
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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 ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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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; |