No paralogue variants have been mapped to residue 1223 for RYR2.
| RYR2 | KDFDVGDGFIPVCSLGVAQVGRMNFGKDVS>T<LKYFTICGLQEGYEPFAVNTNRDITMWLSK | 1253 |
| RYR1 | REIEIGDGFLPVCSLGPGQVGHLNLGQDVS>S<LRFFAICGLQEGFEPFAINMQRPVTTWFSK | 1239 |
| RYR3 | ADYEIENGFVPICCLGLSQIGRMNLGTDAS>T<FKFYTMCGLQEGFEPFAVNMNRDVAMWFSK | 1239 |
| cons | > < |
| Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
|---|---|---|---|---|---|
| p.T1223A | c.3667A>G | Inherited Arrhythmia | CPVT | SIFT: Polyphen: | |
| Reports | Inherited Arrhythmia | CPVT | Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients. PLoS One. 2015 10(6):e0131517. doi: 10.1371/journal.pone.0131517. 26114861 | ||