ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as uncertain significance for Cardiomyopathy

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Total variants: 26
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HGVS dbSNP
NM_000257.4(MYH7):c.4283T>C (p.Leu1428Ser) rs727503244
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.4399C>G (p.Leu1467Val) rs397516214
NM_000257.4(MYH7):c.4427C>T (p.Ser1476Phe) rs1566525169
NM_000257.4(MYH7):c.4454A>G (p.Lys1485Arg) rs1566525134
NM_000257.4(MYH7):c.4541A>G (p.Glu1514Gly) rs1351712658
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=) rs150552664
NM_000257.4(MYH7):c.4588C>T (p.Arg1530Ter) rs397516225
NM_000257.4(MYH7):c.4645-7T>C rs796681603
NM_000257.4(MYH7):c.4660G>A (p.Glu1554Lys)
NM_000257.4(MYH7):c.4668C>A (p.Gly1556=) rs762762532
NM_000257.4(MYH7):c.4679G>A (p.Arg1560Gln) rs730880806
NM_000257.4(MYH7):c.4689G>A (p.Leu1563=) rs770477774
NM_000257.4(MYH7):c.4772T>A (p.Leu1591Gln) rs730880808
NM_000257.4(MYH7):c.4817G>A (p.Arg1606His) rs373514686
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr) rs141122361
NM_000257.4(MYH7):c.4954G>T (p.Asp1652Tyr) rs397516233
NM_000257.4(MYH7):c.4992C>A (p.Asn1664Lys) rs763538103
NM_000257.4(MYH7):c.4992C>T (p.Asn1664=) rs763538103
NM_000257.4(MYH7):c.5013C>T (p.Ile1671=) rs779978846
NM_000257.4(MYH7):c.5071G>A (p.Val1691Met) rs45464193
NM_000257.4(MYH7):c.5158A>G (p.Asn1720Asp) rs1566523039
NM_000257.4(MYH7):c.5178G>A (p.Gln1726=) rs747252861
NM_000257.4(MYH7):c.5181G>A (p.Lys1727=) rs1566523007
NM_000257.4(MYH7):c.5190G>C (p.Met1730Ile) rs1566522989

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