No paralogue variants have been mapped to residue 798 for RYR2.
RYR2 | FRINGQPVQGMFENFNIDGLFFPVVSFSAG>I<KVRFLLGGRHGEFKFLPPPGYAPCYEAVLP | 828 |
RYR1 | FRINGCPVQGVFESFNLDGLFFPVVSFSAG>V<KVRFLLGGRHGEFKFLPPPGYAPCHEAVLP | 816 |
RYR3 | FRINGQPVQGMFENFNTDGLFFPVMSFSAG>V<KVRFLMGGRHGEFKFLPPSGYAPCYEALLP | 815 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.I798T | c.2393T>C | Putative Benign | rs187464772 | SIFT: deleterious Polyphen: possibly damaging | |
p.I798M | c.2394A>G | Putative Benign | rs192876953 | SIFT: deleterious Polyphen: possibly damaging |