No paralogue variants have been mapped to residue 3398 for RYR2.
RYR2 | AFYPLLIRFVDYNRAKWLKEPNPEAEELFR>M<VAEVFIYWSKSHNFKREEQNFVVQNEINNM | 3428 |
RYR1 | ALYPLLIRYVDNNRAQWLTEPNPSAEELFR>M<VGEIFIYWSKSHNFKREEQNFVVQNEINNM | 3467 |
RYR3 | AFYPMLIRYVDNNRSNWLKSPDADSDQLFR>M<VAEVFILWCKSHNFKREEQNFVIQNEINNL | 3324 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.M3398L | c.10192A>T | Putative Benign | SIFT: tolerated Polyphen: probably damaging |