ClinVar Miner

List of variants in gene combination MHRT, MYH7 reported as uncertain significance by Ambry Genetics

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Total variants: 20
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HGVS dbSNP
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.4377G>T (p.Lys1459Asn) rs201307101
NM_000257.4(MYH7):c.4390C>T (p.Gln1464Ter) rs754829218
NM_000257.4(MYH7):c.4402G>A (p.Glu1468Lys) rs876657884
NM_000257.4(MYH7):c.4411C>T (p.Gln1471Ter) rs397516216
NM_000257.4(MYH7):c.4414_4416del (p.Lys1472del) rs1555336672
NM_000257.4(MYH7):c.4450C>A (p.Leu1484Ile) rs1555336651
NM_000257.4(MYH7):c.4499G>A (p.Arg1500Gln) rs121913647
NM_000257.4(MYH7):c.4571A>C (p.His1524Pro) rs767148171
NM_000257.4(MYH7):c.4588C>T (p.Arg1530Ter) rs397516225
NM_000257.4(MYH7):c.4747A>T (p.Met1583Leu) rs1466998230
NM_000257.4(MYH7):c.4772T>A (p.Leu1591Gln) rs730880808
NM_000257.4(MYH7):c.4807G>A (p.Ala1603Thr) rs730880809
NM_000257.4(MYH7):c.4817G>A (p.Arg1606His) rs373514686
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.4895C>A (p.Ala1632Asp) rs1435525455
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr) rs141122361
NM_000257.4(MYH7):c.5066G>A (p.Arg1689His) rs772008016

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