No paralogue variants have been mapped to residue 4724 for RYR1.
RYR1 | EDDDVKGQWDRLVLNTPSFPSNYWDKFVKR>K<VLDKHGDIYGRERIAELLGMDLATLEITAH | 4754 |
RYR2 | SEDDIKGQWDRLVINTQSFPNNYWDKFVKR>K<VMDKYGEFYGRDRISELLGMDKAALDFSDA | 4682 |
RYR3 | SEDDIKGQWDRLVINTPSFPNNYWDKFVKR>K<VINKYGDLYGAERIAELLGLDKNALDFSPV | 4587 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.K4724Q | c.14170A>C | Other Myopathy | rs118192141 | SIFT: Polyphen: | |
Reports | Other Myopathy | Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia. Brain. 2003 126(Pt 11):2341-9. 12937085 | |||
Unknown | Clinical utility gene card for: Multi-minicore disease. Eur J Hum Genet. 2012 20(2). doi: 10.1038/ejhg.2011.180. 22009146 |