ClinVar Miner

List of variants in gene combination MHRT, MYH7 studied for Cardiomyopathy

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Total variants: 47
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HGVS dbSNP
NM_000257.2(MYH7):c.4399C>G (p.Leu1467Val) rs397516214
NM_000257.2(MYH7):c.4557C>T (p.Ser1519=) rs150552664
NM_000257.2(MYH7):c.4908C>T (p.Ala1636=) rs150241539
NM_000257.3(MYH7):c.4283T>C (p.Leu1428Ser) rs727503244
NM_000257.3(MYH7):c.4293C>T (p.Asp1431=) rs45560242
NM_000257.3(MYH7):c.4498C>T (p.Arg1500Trp) rs45544633
NM_000257.3(MYH7):c.4520-3C>T rs549509054
NM_000257.3(MYH7):c.4605C>T (p.Ala1535=) rs746261895
NM_000257.3(MYH7):c.4618C>T (p.Leu1540=) rs368734580
NM_000257.3(MYH7):c.4644+3G>A rs397516226
NM_000257.3(MYH7):c.4660G>A (p.Glu1554Lys)
NM_000257.3(MYH7):c.4679G>A (p.Arg1560Gln) rs730880806
NM_000257.3(MYH7):c.4725G>A (p.Lys1575=) rs45476496
NM_000257.3(MYH7):c.4772T>A (p.Leu1591Gln) rs730880808
NM_000257.3(MYH7):c.4806C>T (p.Asp1602=) rs142034311
NM_000257.3(MYH7):c.4817G>A (p.Arg1606His) rs373514686
NM_000257.3(MYH7):c.4941G>A (p.Gln1647=) rs749154313
NM_000257.3(MYH7):c.4954G>T (p.Asp1652Tyr) rs397516233
NM_000257.3(MYH7):c.4992C>A (p.Asn1664Lys) rs763538103
NM_000257.3(MYH7):c.5071G>A (p.Val1691Met) rs45464193
NM_000257.4(MYH7):c.4321G>T (p.Ala1441Ser) rs745414245
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101
NM_000257.4(MYH7):c.4427C>T (p.Ser1476Phe)
NM_000257.4(MYH7):c.4452C>T (p.Leu1484=) rs61737803
NM_000257.4(MYH7):c.4454A>G (p.Lys1485Arg)
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys) rs3729823
NM_000257.4(MYH7):c.4541A>G (p.Glu1514Gly)
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.4645-7T>C
NM_000257.4(MYH7):c.4668C>A (p.Gly1556=)
NM_000257.4(MYH7):c.4671G>A (p.Lys1557=) rs200601164
NM_000257.4(MYH7):c.4689G>A (p.Leu1563=) rs770477774
NM_000257.4(MYH7):c.4716C>T (p.Ile1572=) rs7140196
NM_000257.4(MYH7):c.4788G>A (p.Ser1596=) rs146858930
NM_000257.4(MYH7):c.4834C>T (p.Leu1612=)
NM_000257.4(MYH7):c.4893C>T (p.His1631=) rs369164804
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr) rs141122361
NM_000257.4(MYH7):c.4974C>T (p.Asp1658=) rs374289523
NM_000257.4(MYH7):c.4992C>T (p.Asn1664=)
NM_000257.4(MYH7):c.5013C>T (p.Ile1671=)
NM_000257.4(MYH7):c.5061G>A (p.Glu1687=)
NM_000257.4(MYH7):c.5106G>A (p.Ala1702=) rs3729830
NM_000257.4(MYH7):c.5158A>G (p.Asn1720Asp)
NM_000257.4(MYH7):c.5178G>A (p.Gln1726=)
NM_000257.4(MYH7):c.5181G>A (p.Lys1727=)
NM_000257.4(MYH7):c.5190G>C (p.Met1730Ile)

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