ClinVar Miner

List of variants in gene combination MHRT, MYH7 studied for Hypertrophic cardiomyopathy

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Total variants: 125
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HGVS dbSNP
NM_000257.3(MYH7):c.4522_4524delGAG (p.Glu1508del) rs397516220
NM_000257.4(MYH7):c.4276G>A (p.Glu1426Lys) rs397516208
NM_000257.4(MYH7):c.4283T>C (p.Leu1428Ser) rs727503244
NM_000257.4(MYH7):c.4286_4288TGG[1] (p.Val1430del) rs1555336747
NM_000257.4(MYH7):c.4290G>T (p.Val1430=) rs372476972
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=) rs45560242
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.4343A>T (p.Asn1448Ile) rs753484341
NM_000257.4(MYH7):c.4347C>G (p.Phe1449Leu)
NM_000257.4(MYH7):c.4353+10G>A rs202205780
NM_000257.4(MYH7):c.4353+5G>A rs200436876
NM_000257.4(MYH7):c.4354-10C>G rs543141581
NM_000257.4(MYH7):c.4354-6G>A rs368078397
NM_000257.4(MYH7):c.4354-7C>T rs370093487
NM_000257.4(MYH7):c.4358T>C (p.Leu1453Pro)
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101
NM_000257.4(MYH7):c.4395G>T (p.Ser1465=) rs397516213
NM_000257.4(MYH7):c.4402G>A (p.Glu1468Lys) rs876657884
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=) rs578166720
NM_000257.4(MYH7):c.4423C>T (p.Arg1475Cys) rs139646545
NM_000257.4(MYH7):c.4440G>T (p.Glu1480Asp)
NM_000257.4(MYH7):c.4450C>A (p.Leu1484Ile) rs1555336651
NM_000257.4(MYH7):c.4452C>T (p.Leu1484=) rs61737803
NM_000257.4(MYH7):c.4459G>A (p.Ala1487Thr)
NM_000257.4(MYH7):c.4460C>T (p.Ala1487Val)
NM_000257.4(MYH7):c.4465_4467GAG[3] (p.Glu1490dup) rs1566525106
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys) rs3729823
NM_000257.4(MYH7):c.4484T>C (p.Leu1495Pro) rs1566525081
NM_000257.4(MYH7):c.4498C>T (p.Arg1500Trp) rs45544633
NM_000257.4(MYH7):c.4499G>C (p.Arg1500Pro) rs121913647
NM_000257.4(MYH7):c.4500G>A (p.Arg1500=) rs199995198
NM_000257.4(MYH7):c.4513C>T (p.Leu1505=) rs139928934
NM_000257.4(MYH7):c.4515G>A (p.Leu1505=) rs397516219
NM_000257.4(MYH7):c.4520-25C>T rs45503601
NM_000257.4(MYH7):c.4520-3C>T rs549509054
NM_000257.4(MYH7):c.4558G>A (p.Gly1520Arg) rs763683589
NM_000257.4(MYH7):c.4566T>C (p.Thr1522=) rs2754155
NM_000257.4(MYH7):c.4567A>G (p.Ile1523Val) rs1555336580
NM_000257.4(MYH7):c.4588C>T (p.Arg1530Ter) rs397516225
NM_000257.4(MYH7):c.4589G>A (p.Arg1530Gln) rs730880803
NM_000257.4(MYH7):c.4590A>G (p.Arg1530=) rs768723855
NM_000257.4(MYH7):c.4605C>T (p.Ala1535=) rs746261895
NM_000257.4(MYH7):c.4618C>T (p.Leu1540=) rs368734580
NM_000257.4(MYH7):c.4630C>A (p.Leu1544Met)
NM_000257.4(MYH7):c.4648T>C (p.Ser1550Pro) rs1555336492
NM_000257.4(MYH7):c.4650C>T (p.Ser1550=) rs1051971790
NM_000257.4(MYH7):c.4659C>T (p.His1553=) rs570079347
NM_000257.4(MYH7):c.4660G>A (p.Glu1554Lys)
NM_000257.4(MYH7):c.4663G>A (p.Glu1555Lys)
NM_000257.4(MYH7):c.4667G>A (p.Gly1556Asp) rs1566524217
NM_000257.4(MYH7):c.4673T>G (p.Ile1558Ser)
NM_000257.4(MYH7):c.4678C>T (p.Arg1560Trp)
NM_000257.4(MYH7):c.4679G>A (p.Arg1560Gln) rs730880806
NM_000257.4(MYH7):c.4687C>G (p.Leu1563Val) rs376843222
NM_000257.4(MYH7):c.4709C>A (p.Ala1570Glu) rs730880807
NM_000257.4(MYH7):c.4716C>T (p.Ile1572=) rs7140196
NM_000257.4(MYH7):c.4717G>A (p.Glu1573Lys) rs750987717
NM_000257.4(MYH7):c.4721G>A (p.Arg1574Gln) rs779715863
NM_000257.4(MYH7):c.4741_4743GAG[1] (p.Glu1582del) rs1555336467
NM_000257.4(MYH7):c.4756G>A (p.Ala1586Thr)
NM_000257.4(MYH7):c.4764C>T (p.Arg1588=) rs1566524059
NM_000257.4(MYH7):c.4775G>A (p.Arg1592Gln) rs1257980330
NM_000257.4(MYH7):c.4783G>A (p.Asp1595Asn) rs1555336453
NM_000257.4(MYH7):c.4788G>A (p.Ser1596=) rs146858930
NM_000257.4(MYH7):c.4803G>A (p.Leu1601=) rs397516228
NM_000257.4(MYH7):c.4806C>T (p.Asp1602=) rs142034311
NM_000257.4(MYH7):c.4807G>C (p.Ala1603Pro) 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.4822C>T (p.Arg1608Cys)
NM_000257.4(MYH7):c.4827C>T (p.Asn1609=) rs587781085
NM_000257.4(MYH7):c.4828G>A (p.Glu1610Lys) rs730880810
NM_000257.4(MYH7):c.4832C>T (p.Ala1611Val) rs757090529
NM_000257.4(MYH7):c.4835T>C (p.Leu1612Pro) rs587779392
NM_000257.4(MYH7):c.4838G>A (p.Arg1613Lys) rs397516230
NM_000257.4(MYH7):c.4844_4846AGA[2] (p.Lys1617del) rs121913648
NM_000257.4(MYH7):c.4845G>T (p.Lys1615Asn) rs1060501446
NM_000257.4(MYH7):c.4855G>A (p.Glu1619Lys) rs45442096
NM_000257.4(MYH7):c.4868A>G (p.Asn1623Ser) rs1306407579
NM_000257.4(MYH7):c.4900C>T (p.Arg1634Cys) rs397516232
NM_000257.4(MYH7):c.4901G>A (p.Arg1634His) rs545875689
NM_000257.4(MYH7):c.4904T>C (p.Met1635Thr) rs145822086
NM_000257.4(MYH7):c.4907C>T (p.Ala1636Val) rs1555336406
NM_000257.4(MYH7):c.4908C>T (p.Ala1636=) rs150241539
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr) rs141122361
NM_000257.4(MYH7):c.4909G>C (p.Ala1637Pro) rs141122361
NM_000257.4(MYH7):c.4935C>A (p.Ser1645Arg)
NM_000257.4(MYH7):c.4954G>T (p.Asp1652Tyr) rs397516233
NM_000257.4(MYH7):c.4966C>G (p.Gln1656Glu) rs1555336334
NM_000257.4(MYH7):c.4974C>T (p.Asp1658=) rs374289523
NM_000257.4(MYH7):c.4979C>A (p.Ala1660Glu) rs1006534868
NM_000257.4(MYH7):c.4985G>T (p.Arg1662Leu) rs370328209
NM_000257.4(MYH7):c.4992C>A (p.Asn1664Lys) rs763538103
NM_000257.4(MYH7):c.4996G>A (p.Asp1666Asn)
NM_000257.4(MYH7):c.5005G>T (p.Glu1669Ter) rs45620235
NM_000257.4(MYH7):c.5005_5007del (p.Glu1669del) rs587779394
NM_000257.4(MYH7):c.5011A>G (p.Ile1671Val) rs1456418703
NM_000257.4(MYH7):c.5014G>A (p.Ala1672Thr)
NM_000257.4(MYH7):c.5019C>T (p.Ile1673=) rs139518691
NM_000257.4(MYH7):c.5020G>A (p.Val1674Met) rs397516235
NM_000257.4(MYH7):c.5026C>T (p.Arg1676Trp) rs753115999
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.5065C>T (p.Arg1689Cys) rs730880915
NM_000257.4(MYH7):c.5066G>A (p.Arg1689His) rs772008016
NM_000257.4(MYH7):c.5071G>A (p.Val1691Met) rs45464193
NM_000257.4(MYH7):c.5085_5086AG[1] (p.Glu1696fs)
NM_000257.4(MYH7):c.5088G>C (p.Glu1696Asp) rs373219734
NM_000257.4(MYH7):c.5102T>A (p.Leu1701Gln)
NM_000257.4(MYH7):c.5106G>A (p.Ala1702=) rs3729830
NM_000257.4(MYH7):c.5113del (p.Glu1705fs) rs878853838
NM_000257.4(MYH7):c.5122G>A (p.Glu1708Lys) rs1057518857
NM_000257.4(MYH7):c.5134C>T (p.Arg1712Trp) rs121913650
NM_000257.4(MYH7):c.5135G>A (p.Arg1712Gln) rs193922390
NM_000257.4(MYH7):c.5157+8G>T rs1555336258
NM_000257.4(MYH7):c.5157G>A (p.Gln1719=) rs769875223
NM_000257.4(MYH7):c.5158-8C>A
NM_000257.4(MYH7):c.5167C>T (p.Leu1723Phe) rs1566523027
NM_000257.4(MYH7):c.5177_5179AGA[3] (p.Lys1729del) rs367543052
NM_000257.4(MYH7):c.5203T>A (p.Ser1735Thr) rs144066768
NM_000257.4(MYH7):c.5206C>T (p.Gln1736Ter)
NM_000257.4(MYH7):c.5208G>C (p.Gln1736His) rs886050416

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