ClinVar Miner

List of variants in gene MYPN reported as pathogenic for Nemaline myopathy 11, autosomal recessive

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
NM_032578.3(MYPN):c.1129C>T (p.Arg377Ter) rs781261060
NM_032578.3(MYPN):c.2003del (p.Asn668fs) rs1057519570
NM_032578.3(MYPN):c.3076-2A>C rs1057519571
NM_032578.3(MYPN):c.3169C>T (p.Arg1057Ter) rs1057519572
NM_032578.3(MYPN):c.3214C>T (p.Arg1072Ter) rs1057519573

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.