No paralogue variants have been mapped to residue 4768 for RYR2.
RYR2 | FFAAHLLDIAMGFKTLRTILSSVTHNGKQL>V<LTVGLLAVVVYLYTVVAFNFFRKFYNKSED | 4798 |
RYR1 | FFAAHLLDIAMGVKTLRTILSSVTHNGKQL>V<MTVGLLAVVVYLYTVVAFNFFRKFYNKSED | 4869 |
RYR3 | FFAAHLLDIAMGFKTLRTILSSVTHNGKQL>V<LTVGLLAVVVYLYTVVAFNFFRKFYNKSED | 4701 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.V4768I | c.14302G>A | Putative Benign | SIFT: Polyphen: |