ClinVar Miner

List of variants in gene combination MHRT, MYH7 studied for not specified

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Total variants: 104
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HGVS dbSNP
NM_000257.4(MYH7):c.4275C>A (p.Ile1425=) rs57680382
NM_000257.4(MYH7):c.4275C>T (p.Ile1425=) rs57680382
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.4290G>T (p.Val1430=) rs372476972
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=) rs45560242
NM_000257.4(MYH7):c.4326G>A (p.Leu1442=) rs727503243
NM_000257.4(MYH7):c.4330A>G (p.Lys1444Glu) rs397516210
NM_000257.4(MYH7):c.4348G>A (p.Asp1450Asn) rs397516211
NM_000257.4(MYH7):c.4353+10G>A rs202205780
NM_000257.4(MYH7):c.4353+13T>G rs587781084
NM_000257.4(MYH7):c.4353+17G>A rs45581933
NM_000257.4(MYH7):c.4353+42G>A rs3729822
NM_000257.4(MYH7):c.4353+6C>T rs765398896
NM_000257.4(MYH7):c.4354-2A>C rs727504734
NM_000257.4(MYH7):c.4354-6G>A rs368078397
NM_000257.4(MYH7):c.4354-7C>T rs370093487
NM_000257.4(MYH7):c.4362C>G (p.Ala1454=) rs727505281
NM_000257.4(MYH7):c.4363G>A (p.Glu1455Lys) rs876661373
NM_000257.4(MYH7):c.4371G>A (p.Lys1457=) rs1555336697
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101
NM_000257.4(MYH7):c.4388C>T (p.Ser1463Leu) rs890401818
NM_000257.4(MYH7):c.4395G>T (p.Ser1465=) rs397516213
NM_000257.4(MYH7):c.4399C>G (p.Leu1467Val) rs397516214
NM_000257.4(MYH7):c.4402G>A (p.Glu1468Lys) rs876657884
NM_000257.4(MYH7):c.4402G>C (p.Glu1468Gln) rs876657884
NM_000257.4(MYH7):c.4408T>C (p.Ser1470Pro) rs397516215
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=) rs578166720
NM_000257.4(MYH7):c.4411C>T (p.Gln1471Ter) rs397516216
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.4452C>T (p.Leu1484=) rs61737803
NM_000257.4(MYH7):c.4470G>C (p.Glu1490Asp) rs730880911
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys) rs3729823
NM_000257.4(MYH7):c.4481A>T (p.His1494Leu) rs727505329
NM_000257.4(MYH7):c.4487A>C (p.Glu1496Ala) rs397516218
NM_000257.4(MYH7):c.4513C>T (p.Leu1505=) rs139928934
NM_000257.4(MYH7):c.4515G>T (p.Leu1505=) rs397516219
NM_000257.4(MYH7):c.4519+1G>C rs876661374
NM_000257.4(MYH7):c.4520-25C>T rs45503601
NM_000257.4(MYH7):c.4525A>C (p.Ile1509Leu) rs397516221
NM_000257.4(MYH7):c.4537A>T (p.Thr1513Ser) rs397516222
NM_000257.4(MYH7):c.4540G>A (p.Glu1514Lys) rs397516223
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=) rs150552664
NM_000257.4(MYH7):c.4566T>C (p.Thr1522=) rs2754155
NM_000257.4(MYH7):c.4588C>T (p.Arg1530Ter) rs397516225
NM_000257.4(MYH7):c.4618C>T (p.Leu1540=) rs368734580
NM_000257.4(MYH7):c.4644+3G>A rs397516226
NM_000257.4(MYH7):c.4644+7G>C rs1555336564
NM_000257.4(MYH7):c.4645-16C>T rs778453839
NM_000257.4(MYH7):c.4645-17C>T rs1555336497
NM_000257.4(MYH7):c.4659C>T (p.His1553=) rs570079347
NM_000257.4(MYH7):c.4663G>C (p.Glu1555Gln) rs727505176
NM_000257.4(MYH7):c.4671G>A (p.Lys1557=) rs200601164
NM_000257.4(MYH7):c.4679G>A (p.Arg1560Gln) rs730880806
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.4720C>T (p.Arg1574Trp) rs397516227
NM_000257.4(MYH7):c.4721G>A (p.Arg1574Gln) rs779715863
NM_000257.4(MYH7):c.4725G>A (p.Lys1575=) rs45476496
NM_000257.4(MYH7):c.4788G>A (p.Ser1596=) rs146858930
NM_000257.4(MYH7):c.4800C>T (p.Ser1600=) rs1057521761
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.4816C>T (p.Arg1606Cys) rs200530211
NM_000257.4(MYH7):c.4817G>A (p.Arg1606His) rs373514686
NM_000257.4(MYH7):c.4826_4828delinsGCCGCAACC (p.Asn1609_Glu1610delinsSerArgAsnGln) rs1555336439
NM_000257.4(MYH7):c.4827C>T (p.Asn1609=) rs587781085
NM_000257.4(MYH7):c.4832C>T (p.Ala1611Val) rs757090529
NM_000257.4(MYH7):c.4834C>G (p.Leu1612Val) rs397516229
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.4869T>C (p.Asn1623=) rs1448315071
NM_000257.4(MYH7):c.4893C>T (p.His1631=) rs369164804
NM_000257.4(MYH7):c.4900C>T (p.Arg1634Cys) rs397516232
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr) rs141122361
NM_000257.4(MYH7):c.4911C>T (p.Ala1637=) rs151113658
NM_000257.4(MYH7):c.4915G>A (p.Ala1639Thr) rs864309553
NM_000257.4(MYH7):c.4941G>A (p.Gln1647=) rs749154313
NM_000257.4(MYH7):c.4953+13A>T rs373509029
NM_000257.4(MYH7):c.4953+17G>A rs376604168
NM_000257.4(MYH7):c.4954-14C>G rs727505070
NM_000257.4(MYH7):c.4954-14C>T rs727505070
NM_000257.4(MYH7):c.4954G>T (p.Asp1652Tyr) rs397516233
NM_000257.4(MYH7):c.4974C>T (p.Asp1658=) rs374289523
NM_000257.4(MYH7):c.4985G>A (p.Arg1662His) rs370328209
NM_000257.4(MYH7):c.4992C>T (p.Asn1664=) rs763538103
NM_000257.4(MYH7):c.5015_5020del (p.Ala1672_Ile1673del) rs397516234
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.5065C>T (p.Arg1689Cys) rs730880915
NM_000257.4(MYH7):c.5067_5079delinsGGCCGTGGAAGAA (p.Val1692Glu) rs727505033
NM_000257.4(MYH7):c.5070C>G (p.Ala1690=) rs764844610
NM_000257.4(MYH7):c.5071G>A (p.Val1691Met) rs45464193
NM_000257.4(MYH7):c.5088G>C (p.Glu1696Asp) rs373219734
NM_000257.4(MYH7):c.5096G>A (p.Arg1699Gln) rs146778113
NM_000257.4(MYH7):c.5106G>A (p.Ala1702=) rs3729830
NM_000257.4(MYH7):c.5110C>T (p.Gln1704Ter) rs727504844
NM_000257.4(MYH7):c.5115G>A (p.Glu1705=) rs397516239
NM_000257.4(MYH7):c.5134C>T (p.Arg1712Trp) rs121913650
NM_000257.4(MYH7):c.5156A>G (p.Gln1719Arg) rs727504403
NM_000257.4(MYH7):c.5158-15C>T rs369453980
NM_000257.4(MYH7):c.5191G>A (p.Asp1731Asn) rs876657885
NM_000257.4(MYH7):c.5192A>T (p.Asp1731Val) rs397516240

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