ClinVar Miner

List of variants in gene MYH14 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_001145809.2(MYH14):c.2161C>T (p.Arg721Cys) rs373929652
NM_001145809.2(MYH14):c.2459G>A (p.Arg820His) rs370765705
NM_001145809.2(MYH14):c.3863A>T (p.Glu1288Val) rs1555773701
NM_001145809.2(MYH14):c.5176C>T (p.Arg1726Trp) rs372062358
NM_001145809.2(MYH14):c.5953C>T (p.Arg1985Trp) rs369147236
NM_001145809.2(MYH14):c.6035_6037AGG[1] (p.Glu2013del) rs867351302
NM_001145809.2(MYH14):c.752C>A (p.Pro251His) rs779215539
NM_001145809.2(MYH14):c.838G>A (p.Val280Ile) rs202246093

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.