ClinVar Miner

List of variants in gene MYPN reported as likely benign by Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP
NM_032578.3(MYPN):c.1104C>T (p.Gly368=) rs144764983
NM_032578.3(MYPN):c.1134C>T (p.Ile378=) rs145701607
NM_032578.3(MYPN):c.1236C>A (p.Thr412=) rs151220474
NM_032578.3(MYPN):c.1245+20A>G rs111634581
NM_032578.3(MYPN):c.1246-19G>A rs75739924
NM_032578.3(MYPN):c.1293C>A (p.Ile431=) rs147184158
NM_032578.3(MYPN):c.1460-14T>A rs201156035
NM_032578.3(MYPN):c.1662A>C (p.Ala554=) rs71584488
NM_032578.3(MYPN):c.1725A>G (p.Lys575=) rs143213775
NM_032578.3(MYPN):c.1893G>A (p.Arg631=) rs145440469
NM_032578.3(MYPN):c.1935C>T (p.Pro645=) rs71535754
NM_032578.3(MYPN):c.2880T>G (p.Ser960=) rs146028308
NM_032578.3(MYPN):c.2925+9G>C rs12241644
NM_032578.3(MYPN):c.3075+20C>T rs377273417
NM_032578.3(MYPN):c.3720C>T (p.Asp1240=) rs146280945
NM_032578.3(MYPN):c.3735G>T (p.Thr1245=) rs184347775
NM_032578.3(MYPN):c.3792C>T (p.Tyr1264=) rs142307556
NM_032578.3(MYPN):c.395C>T (p.Pro132Leu) rs201203517

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.