No paralogue variants have been mapped to residue 3521 for RYR1.
RYR1 | QERTKKKRRGDRYSVQTSLIVATLKKMLPI>G<LNMCAPTDQDLITLAKTRYALKDTDEEVRE | 3551 |
RYR2 | QERKKMKRKGDRYSMQTSLIVAALKRLLPI>G<LNICAPGDQELIALAKNRFSLKDTEDEVRD | 3507 |
RYR3 | QERKKTKRRGDLYSIQTSLIVAALKKMLPI>G<LNMCTPGDQELISLAKSRYSHRDTDEEVRE | 3408 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.G3521C | c.10561G>T | Other Myopathy | SIFT: Polyphen: | ||
Reports | Other Myopathy | Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization. Neuropathol Appl Neurobiol. 2011 37(3):271-84. doi: 10.1111/j.1365-2990.2010.01149. 21062345 |