Paralogue Annotation for RYR1 residue 4717

Residue details

Gene: RYR1
Reference Sequences: Ensembl variant: ENST00000359596 / ENSP00000352608
Amino Acid Position: 4717
Reference Amino Acid: W - Tryptophan
Protein Domain:


Paralogue Variants mapped to RYR1 residue 4717

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR2W4645RCatecholaminergic polymorphic ventricular tachycarHigh9 19398417, 24025405, 25525159, 27114410

To assess whether the paralogue annotation here confidently predicts that variation at this residue is pathogenic, it is important to check the reports in the Pubmed links above to ascertain that the mutations in these paralogues have been proved likely to be disease-causing. It is also important to check that the direction of effect of the variant in the paralogue is compatible with your observed phenotype in RYR1.



RYR1LYITEQPEDDDVKGQWDRLVLNTPSFPSNY>W<DKFVKRKVLDKHGDIYGRERIAELLGMDLA4747
RYR2LYITEQPSEDDIKGQWDRLVINTQSFPNNY>W<DKFVKRKVMDKYGEFYGRDRISELLGMDKA4675
RYR3LYITEQPSEDDIKGQWDRLVINTPSFPNNY>W<DKFVKRKVINKYGDLYGAERIAELLGLDKN4580
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.W4717Rc.14149T>C Putative BenignSIFT:
Polyphen: