No paralogue variants have been mapped to residue 774 for RYR1.
RYR1 | SCCLDLSVPSISFRINGCPVQGVFESFNLD>G<LFFPVVSFSAGVKVRFLLGGRHGEFKFLPP | 804 |
RYR2 | SCCLDLSAPSISFRINGQPVQGMFENFNID>G<LFFPVVSFSAGIKVRFLLGGRHGEFKFLPP | 816 |
RYR3 | SCCLDLGVPSISFRINGQPVQGMFENFNTD>G<LFFPVMSFSAGVKVRFLMGGRHGEFKFLPP | 803 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.G774R | c.2320G>A | Putative Benign | rs147918857 | SIFT: Polyphen: probably damaging |