ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP
NM_002474.3(MYH11):c.3973C>G (p.Gln1325Glu) rs150033906
NM_002474.3(MYH11):c.4177G>C (p.Gly1393Arg) rs143620567
NM_002474.3(MYH11):c.4240_4242delinsACG (p.Ala1414Thr) rs794728676
NM_002474.3(MYH11):c.4327G>A (p.Val1443Met) rs141262029
NM_002474.3(MYH11):c.4578+5G>C rs1555552121
NM_002474.3(MYH11):c.4603C>T (p.Arg1535Trp) rs143402648
NM_002474.3(MYH11):c.4628A>C (p.Glu1543Ala) rs1555551985
NM_002474.3(MYH11):c.4790A>G (p.Gln1597Arg) rs534983279
NM_002474.3(MYH11):c.4791+5G>A rs376779423
NM_002474.3(MYH11):c.4861A>C (p.Lys1621Gln) rs34321232
NM_002474.3(MYH11):c.5095G>A (p.Ala1699Thr) rs200410021
NM_002474.3(MYH11):c.5261C>T (p.Ala1754Val) rs904032269
NM_002474.3(MYH11):c.5302C>G (p.Gln1768Glu) rs901502893
NM_002474.3(MYH11):c.5336C>A (p.Thr1779Lys) rs201960644
NM_002474.3(MYH11):c.5470G>A (p.Ala1824Thr) rs147710374
NM_002474.3(MYH11):c.5499G>C (p.Glu1833Asp) rs145252402
NM_002474.3(MYH11):c.5788C>T (p.Arg1930Ter) rs772670393

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.