ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP
NM_002474.3(MYH11):c.3874G>A (p.Val1292Ile) rs151058774
NM_002474.3(MYH11):c.3897C>T (p.Ala1299=) rs190546350
NM_002474.3(MYH11):c.4293C>T (p.Asp1431=) rs143588920
NM_002474.3(MYH11):c.4861A>C (p.Lys1621Gln) rs34321232
NM_002474.3(MYH11):c.5062G>C (p.Asp1688His) rs1239423939
NM_002474.3(MYH11):c.5176G>A (p.Ala1726Thr) rs376154041
NM_002474.3(MYH11):c.5364G>A (p.Gln1788=) rs1064797209
NM_002474.3(MYH11):c.5499G>C (p.Glu1833Asp) rs145252402

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.