Paralogue Annotation for RYR1 residue 2364

Residue details

Gene: RYR1
Reference Sequences: Ensembl variant: ENST00000359596 / ENSP00000352608
Amino Acid Position: 2364
Reference Amino Acid: F - Phenylalanine
Protein Domain:


Paralogue Variants mapped to RYR1 residue 2364

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR2F2331SVentricular tachycardia, polymorphicHigh9 16436635, 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.



RYR1FLRFAVFVNGESVEENANVVVRLLIRKPEC>F<GPALRGEGGSGLLAAIEEAIRISEDPARDG2394
RYR2FLRFAVFCNGESVEENANVVVRLLIRRPEC>F<GPALRGEGGNGLLAAMEEAIKIAEDPSRDG2361
RYR3FLRFAVFVNSESVEENASVVVKLLIRRPEC>F<GPALRGEGGNGLLAAMQGAIKISENPALDL2258
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.F2364Vc.7090T>G Other MyopathySIFT:
Polyphen:
ReportsOther Myopathy Mutations in RYR1 in malignant hyperthermia and central core disease. Hum Mutat. 2006 27(10):977-89. 16917943