Paralogue Annotation for RYR2 residue 4815

Residue details

Gene: RYR2
Reference Sequences: LRG: LRG_402, Ensembl variant: ENST00000366574 / ENSP00000355533
Amino Acid Position: 4815
Reference Amino Acid: F - Phenylalanine
Protein Domain: Transmembrane region


Paralogue Variants mapped to RYR2 residue 4815

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR1F4886LMyopathy, congenitalHigh9 22473935

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 RYR2.



RYR2AFNFFRKFYNKSEDGDTPDMKCDDMLTCYM>F<HMYVGVRAGGGIGDEIEDPAGDEYEIYRII4845
RYR1AFNFFRKFYNKSEDEDEPDMKCDDMMTCYL>F<HMYVGVRAGGGIGDEIEDPAGDEYELYRVV4916
RYR3AFNFFRKFYNKSEDDDEPDMKCDDMMTCYL>F<HMYVGVRAGGGIGDEIEDPAGDPYEMYRIV4748
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR2

There are currently no reported variants at residue 4815 for RYR2.