No paralogue variants have been mapped to residue 3851 for RYR2.
| RYR2 | -----GEKVLQDDEFTCDLFRFLQLLCEGH>N<SDFQNYLRTQTGNNTTVNIIISTVDYLLRV | 3881 |
| RYR1 | INRQNGEKVMADDEFTQDLFRFLQLLCEGH>N<NDFQNYLRTQTGNTTTINIIICTVDYLLRL | 3925 |
| RYR3 | IVRERGEKVLQNDEFTRDLFRFLQLLCEGH>N<SDFQNFLRTQMGNTTTVNVIISTVDYLLRL | 3777 |
| cons | > < |
| Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
|---|---|---|---|---|---|
| p.N3851S | c.11552A>G | Putative Benign | SIFT: deleterious Polyphen: probably damaging |