Paralogue Annotation for RYR2 residue 850

Residue details

Gene: RYR2
Reference Sequences: LRG: LRG_402, Ensembl variant: ENST00000366574 / ENSP00000355533
Amino Acid Position: 850
Reference Amino Acid: L - Leucine
Protein Domain: Cytoplasmic region

Paralogue Variants mapped to RYR2 residue 850

Paralogue	Variant	Associated Disease	Mapping Quality	Consensus	Pubmed
RYR1	L838P	Central core disease	High	9	25960145

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.

RYR2	APCYEAVLPKEKLKVEHSREYKQERTYTRD>L<LGPTVSLTQAAFTPIPVDTSQIVLPPHLER	880
RYR1	APCHEAVLPRERLHLEPIKEYRREGPRGPH>L<VGPSRCLSHTDFVPCPVDTVQIVLPPHLER	868
RYR3	APCYEALLPKEKMRLEPVKEYKRDADGIRD>L<LGTTQFLSQASFIPCPVDTSQVILPPHLEK	867
cons	> <

See full Alignment of Paralogues

Known Variants in RYR2

There are currently no reported variants at residue 850 for RYR2.