Paralogue Annotation for RYR1 residue 3920

Residue details

Gene: RYR1
Reference Sequences: Ensembl variant: ENST00000359596 / ENSP00000352608
Amino Acid Position: 3920
Reference Amino Acid: D - Aspartate
Protein Domain:

Paralogue Variants mapped to RYR1 residue 3920

Paralogue	Variant	Associated Disease	Mapping Quality	Consensus	Pubmed
RYR2	D3876E	Catecholaminergic polymorphic ventricular tachycar	High	9	23595086

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.

RYR1	LCEGHNNDFQNYLRTQTGNTTTINIIICTV>D<YLLRLQESISDFYWYYSGKDVIEEQGKRNF	3950
RYR2	LCEGHNSDFQNYLRTQTGNNTTVNIIISTV>D<YLLRVQESISDFYWYYSGKDVIDEQGQRNF	3906
RYR3	LCEGHNSDFQNFLRTQMGNTTTVNVIISTV>D<YLLRLQESISDFYWYYSGKDIIDESGQHNF	3802
cons	> <

See full Alignment of Paralogues

Known Variants in RYR1

There are currently no reported variants at residue 3920 for RYR1.