Paralogue Annotation for RYR1 residue 2287

Residue details

Gene: RYR1
Reference Sequences: Ensembl variant: ENST00000359596 / ENSP00000352608
Amino Acid Position: 2287
Reference Amino Acid: A - Alanine
Protein Domain:


Paralogue Variants mapped to RYR1 residue 2287

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR2A2254VVentricular tachycardia, polymorphicHigh9 15998675, 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.



RYR1NSGIG--L-GMQGSTPLDVAAASVIDNNEL>A<LALQEQDLEKVVSYLAGCGLQSCPMLVAKG2317
RYR2NSSVGLASPAMRGSTPLDVAAASVMDNNEL>A<LALREPDLEKVVRYLAGCGLQSCQMLVSKG2284
RYR3NSSVGLASPSMRGSTPLDVAASSVMDNNEL>A<LSLEEPDLEKVVTYLAGCGLQSCPMLLAKG2181
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.A2287Tc.6859G>A Putative BenignSIFT:
Polyphen:
p.A2287Dc.6860C>A Putative BenignSIFT:
Polyphen: