ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
Download table as spreadsheet
HGVS dbSNP
NM_000257.4(MYH7):c.4270G>A (p.Glu1424Lys) rs730880798
NM_000257.4(MYH7):c.4285A>T (p.Met1429Leu)
NM_000257.4(MYH7):c.4294G>A (p.Val1432Ile) rs144200285
NM_000257.4(MYH7):c.4300C>T (p.Arg1434Cys) rs730880800
NM_000257.4(MYH7):c.4321G>T (p.Ala1441Ser) rs745414245
NM_000257.4(MYH7):c.4332G>A (p.Lys1444=) rs1064797183
NM_000257.4(MYH7):c.4343A>T (p.Asn1448Ile) rs753484341
NM_000257.4(MYH7):c.4353+5G>A rs200436876
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101
NM_000257.4(MYH7):c.4389G>A (p.Ser1463=) rs781203524
NM_000257.4(MYH7):c.4423C>T (p.Arg1475Cys) rs139646545
NM_000257.4(MYH7):c.4436C>T (p.Thr1479Ile) rs397516217
NM_000257.4(MYH7):c.4441C>T (p.Leu1481Phe) rs767666398
NM_000257.4(MYH7):c.4532A>C (p.Asp1511Ala) rs730880802
NM_000257.4(MYH7):c.4588C>G (p.Arg1530Gly) rs397516225
NM_000257.4(MYH7):c.4589G>A (p.Arg1530Gln) rs730880803
NM_000257.4(MYH7):c.4606G>T (p.Glu1536Ter) rs779315151
NM_000257.4(MYH7):c.4644+5G>C rs730880797
NM_000257.4(MYH7):c.4649C>T (p.Ser1550Phe) rs730880912
NM_000257.4(MYH7):c.4679G>A (p.Arg1560Gln) rs730880806
NM_000257.4(MYH7):c.4680G>A (p.Arg1560=) rs771236158
NM_000257.4(MYH7):c.4681G>C (p.Ala1561Pro) rs1064796334
NM_000257.4(MYH7):c.4689G>A (p.Leu1563=) rs770477774
NM_000257.4(MYH7):c.4707G>T (p.Lys1569Asn) rs199557822
NM_000257.4(MYH7):c.4709C>A (p.Ala1570Glu) rs730880807
NM_000257.4(MYH7):c.4807G>A (p.Ala1603Thr) rs730880809
NM_000257.4(MYH7):c.4816C>T (p.Arg1606Cys) rs200530211
NM_000257.4(MYH7):c.4817G>A (p.Arg1606His) rs373514686
NM_000257.4(MYH7):c.4831G>T (p.Ala1611Ser) rs730880913
NM_000257.4(MYH7):c.4838G>A (p.Arg1613Lys) rs397516230
NM_000257.4(MYH7):c.4864C>T (p.Leu1622Phe) rs397516231
NM_000257.4(MYH7):c.4872G>T (p.Glu1624Asp) rs766561921
NM_000257.4(MYH7):c.4900C>T (p.Arg1634Cys) rs397516232
NM_000257.4(MYH7):c.4904T>C (p.Met1635Thr) rs145822086
NM_000257.4(MYH7):c.4911C>T (p.Ala1637=) rs151113658
NM_000257.4(MYH7):c.4916C>T (p.Ala1639Val) rs1195157116
NM_000257.4(MYH7):c.4954G>T (p.Asp1652Tyr) rs397516233
NM_000257.4(MYH7):c.4979C>A (p.Ala1660Glu) rs1006534868
NM_000257.4(MYH7):c.5005G>T (p.Glu1669Ter) rs45620235
NM_000257.4(MYH7):c.5017A>G (p.Ile1673Val) rs753907340
NM_000257.4(MYH7):c.5027G>A (p.Arg1676Gln) rs1451176863
NM_000257.4(MYH7):c.5029C>T (p.Arg1677Cys) rs377461670
NM_000257.4(MYH7):c.5030G>A (p.Arg1677His) rs730880914
NM_000257.4(MYH7):c.5110C>T (p.Gln1704Ter) rs727504844
NM_000257.4(MYH7):c.5120T>C (p.Ile1707Thr) rs730880811
NM_000257.4(MYH7):c.5139G>A (p.Val1713=) rs369562442
NM_000257.4(MYH7):c.5203T>A (p.Ser1735Thr) rs144066768

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.