Paralogue Annotation for RYR1 residue 4703

Residue details

Gene: RYR1
Reference Sequences: Ensembl variant: ENST00000359596 / ENSP00000352608
Amino Acid Position: 4703
Reference Amino Acid: D - Aspartate
Protein Domain:


Paralogue Variants mapped to RYR1 residue 4703

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR2D4631VCatecholaminergic polymorphic ventricular tachycarHigh9 24978818

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.



RYR1KREKELARKLEFDGLYITEQPEDDDVKGQW>D<RLVLNTPSFPSNYWDKFVKRKVLDKHGDIY4733
RYR2KREKEVARKLEFDGLYITEQPSEDDIKGQW>D<RLVINTQSFPNNYWDKFVKRKVMDKYGEFY4661
RYR3KREKEIARKLEFDGLYITEQPSEDDIKGQW>D<RLVINTPSFPNNYWDKFVKRKVINKYGDLY4566
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR1

There are currently no reported variants at residue 4703 for RYR1.