Paralogue Annotation for RYR1 residue 1001

Residue details

Gene: RYR1
Reference Sequences: Ensembl variant: ENST00000359596 / ENSP00000352608
Amino Acid Position: 1001
Reference Amino Acid: G - Glycine
Protein Domain:


Paralogue Variants mapped to RYR1 residue 1001

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR2R1013QCatecholaminergic polymorphic ventricular tachycarMedium7 19926015, 24025405, 24055113, 25637381, 27153395, 26332594

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.



RYR1LSHVRLTPAQTTLVDRLAENGHNVWARDRV>G<QGWSYSAVQDIPARRNPRLVPYRLLDEATK1031
RYR2LSFIKLTPSQEAMVDKLAENAHNVWARDRI>R<QGWTYGIQQDVKNRRNPRLVPYTLLDDRTK1043
RYR3LSDVKLLPPQEILVDKLAENAHNVWAKDRI>K<QGWTYGIQQDLKNKRNPRLVPYALLDERTK1030
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.G1001Sc.3001G>A Putative BenignSIFT:
Polyphen: