No paralogue variants have been mapped to residue 774 for RYR2.
RYR2 | PNQHLLRTDDVISCCLDLSAPSISFRINGQ>P<VQGMFENFNIDGLFFPVVSFSAGIKVRFLL | 804 |
RYR1 | PGQHLLAPEDVISCCLDLSVPSISFRINGC>P<VQGVFESFNLDGLFFPVVSFSAGVKVRFLL | 792 |
RYR3 | INQHLLRSDDVVSCCLDLGVPSISFRINGQ>P<VQGMFENFNTDGLFFPVMSFSAGVKVRFLM | 791 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.P774T | c.2320C>A | Putative Benign | SIFT: Polyphen: |