No paralogue variants have been mapped to residue 899 for RYR1.
RYR1 | IREKLAENIHELWALTRIEQGWTYGPVRDD>N<KRLHPCLVDFHSLPEPERNYNLQMSGETLK | 929 |
RYR2 | IREKLAENIHELWVMNKIELGWQYGPVRDD>N<KRQHPCLVEFSKLPEQERNYNLQMSLETLK | 941 |
RYR3 | IRDRLAENIHELWGMNKIELGWTFGKIRDD>N<KRQHPCLVEFSKLPETEKNYNLQMSTETLK | 928 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.N899K | c.2697C>A | Putative Benign | rs201401814 | SIFT: Polyphen: probably damaging | |
p.N899K | c.2697C>G | Putative Benign | SIFT: Polyphen: |