Paralogue Annotation for RYR2 residue 2156

Residue details

Gene: RYR2
Reference Sequences: LRG: LRG_402, Ensembl variant: ENST00000366574 / ENSP00000355533
Amino Acid Position: 2156
Reference Amino Acid: Y - Tyrosine
Protein Domain: Cytoplasmic region

Paralogue Variants mapped to RYR2 residue 2156

No paralogue variants have been mapped to residue 2156 for RYR2.

RYR2	IRSLLSVRMGKEEEKLMIRGLGDIMNNKVF>Y<QHPNLMRALGMHETVMEVMVNVLGGGESKE	2186
RYR1	IRSLLIVQMGPQEENLMIQSIGNIMNNKVF>Y<QHPNLMRALGMHETVMEVMVNVLGGGESKE	2222
RYR3	IRSLLSVRMGKEEELLMINGLGDIMNNKVF>Y<QHPNLMRVLGMHETVMEVMVNVLGT-EKSQ	2083
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See full Alignment of Paralogues

Known Variants in RYR2

Protein	CDS	Disease Classification	Disease	dbSNP links	Effect Prediction
p.Y2156C	c.6467A>G	Putative Benign			SIFT: deleterious Polyphen: probably damaging
Reports		Putative Benign		The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis. J Am Coll Cardiol. 2009 54(22):2065-74. 19926015