No paralogue variants have been mapped to residue 3896 for RYR2.
RYR2 | TTVNIIISTVDYLLRVQESISDFYWYYSGK>D<VIDEQGQRNFSKAIQVAKQVFNTLTEYIQG | 3926 |
RYR1 | TTINIIICTVDYLLRLQESISDFYWYYSGK>D<VIEEQGKRNFSKAMSVAKQVFNSLTEYIQG | 3970 |
RYR3 | TTVNVIISTVDYLLRLQESISDFYWYYSGK>D<IIDESGQHNFSKALAVTKQIFNSLTEYIQG | 3822 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.D3896N | c.11686G>A | Putative Benign | SIFT: Polyphen: probably damaging |