Paralogue Annotation for RYR1 residue 1242

Residue details

Gene: RYR1
Reference Sequences: Ensembl variant: ENST00000359596 / ENSP00000352608
Amino Acid Position: 1242
Reference Amino Acid: P - Proline
Protein Domain:


Paralogue Variants mapped to RYR1 residue 1242

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR2P1256TCatecholaminergic polymorphic ventricular tachycarHigh5 26114861

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.



RYR1FFAICGLQEGFEPFAINMQRPVTTWFSKGL>P<QFEPVPLEHPHYEVSRVDGTVDTPPCLRLT1272
RYR2YFTICGLQEGYEPFAVNTNRDITMWLSKRL>P<QFLQVPSNHEHIEVTRIDGTIDSSPCLKVT1286
RYR3FYTMCGLQEGFEPFAVNMNRDVAMWFSKRL>P<TFVNVPKDHPHIEVMRIDGTMDSPPCLKVT1272
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.P1242Hc.3725C>A Putative BenignSIFT:
Polyphen: