ClinVar Miner

List of variants in gene MYPN reported as likely benign by Biesecker Lab/Human Development Section,National Institutes of Health

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_032578.3(MYPN):c.1790G>A (p.Arg597His) rs150911078
NM_032578.3(MYPN):c.2863C>T (p.Arg955Trp) rs149887823
NM_032578.3(MYPN):c.3335C>T (p.Pro1112Leu) rs71534278
NM_032578.3(MYPN):c.3846T>A (p.Ser1282Arg) rs147659164
NM_032578.3(MYPN):c.59A>G (p.Tyr20Cys) rs140148105
NM_032578.3(MYPN):c.952G>A (p.Val318Ile) rs112518450

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.