Paralogue Annotation for RYR1 residue 3816

Residue details

Gene: RYR1
Reference Sequences: Ensembl variant: ENST00000359596 / ENSP00000352608
Amino Acid Position: 3816
Reference Amino Acid: L - Leucine
Protein Domain:


Paralogue Variants mapped to RYR1 residue 3816

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR2L3778FVentricular tachycardia, polymorphicHigh7 12093772, 24025405

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.



RYR1KGETGAMVSSTLKLGISILNGGNAEVQQKM>L<DYLKDKKEVGFFQSIQALMQTCSVLDLNAF3846
RYR2KGETGPMVAATLKLGIAILNGGNSTVQQKM>L<DYLKEKKDVGFFQSLAGLMQSCSVLDLNAF3808
RYR3KGEMSPMVVETLKLGIAILNGGNAGVQQKM>L<DYLKEKKDAGFFQSLSGLMQSCSVLDLNAF3698
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR1

There are currently no reported variants at residue 3816 for RYR1.