ClinVar Miner

List of variants reported as not provided by Leiden Muscular Dystrophy (MYL3)

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 14
Download table as spreadsheet
NM_000258.2(MYL3):c.*27G>A rs199474710
NM_000258.2(MYL3):c.167A>G (p.Glu56Gly) rs199474702
NM_000258.2(MYL3):c.170C>G (p.Ala57Gly) rs139794067
NM_000258.2(MYL3):c.281G>A (p.Arg94His) rs199474703
NM_000258.2(MYL3):c.382G>T (p.Gly128Cys) rs199474704
NM_000258.2(MYL3):c.427G>A (p.Glu143Lys) rs104893750
NM_000258.2(MYL3):c.445A>G (p.Met149Val) rs104893748
NM_000258.2(MYL3):c.454G>A (p.Glu152Lys) rs199474705
NM_000258.2(MYL3):c.461G>A (p.Arg154His) rs104893749
NM_000258.2(MYL3):c.463C>G (p.His155Asp) rs199474706
NM_000258.2(MYL3):c.466G>A (p.Val156Met) rs199474707
NM_000258.2(MYL3):c.482-2A>G rs111617556
NM_000258.2(MYL3):c.517A>G (p.Met173Val) rs199474708
NM_000258.2(MYL3):c.559+6C>T rs199474709

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.