ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance by Blueprint Genetics

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Total variants: 38
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HGVS dbSNP
NM_000257.4(MYH7):c.1164G>A (p.Met388Ile)
NM_000257.4(MYH7):c.1193G>A (p.Gly398Glu) rs730880158
NM_000257.4(MYH7):c.1258G>A (p.Val420Met)
NM_000257.4(MYH7):c.1315A>T (p.Met439Leu) rs370310929
NM_000257.4(MYH7):c.1396G>A (p.Glu466Lys) rs4981473
NM_000257.4(MYH7):c.161G>A (p.Arg54Gln) rs397516117
NM_000257.4(MYH7):c.1632C>T (p.Thr544=) rs587781089
NM_000257.4(MYH7):c.1699C>T (p.Arg567Cys) rs771771163
NM_000257.4(MYH7):c.1772T>C (p.Ile591Thr) rs775089432
NM_000257.4(MYH7):c.1820G>A (p.Gly607Asp) rs869025479
NM_000257.4(MYH7):c.1884delinsAC (p.Asp628fs)
NM_000257.4(MYH7):c.2206A>G (p.Ile736Val) rs397516138
NM_000257.4(MYH7):c.2293T>G (p.Phe765Val)
NM_000257.4(MYH7):c.2534G>A (p.Arg845Lys)
NM_000257.4(MYH7):c.2606G>A (p.Arg869His) rs202141173
NM_000257.4(MYH7):c.2613G>T (p.Lys871Asn) rs869025480
NM_000257.4(MYH7):c.2765T>C (p.Met922Thr)
NM_000257.4(MYH7):c.2822G>A (p.Arg941His)
NM_000257.4(MYH7):c.29G>C (p.Gly10Ala) rs730880826
NM_000257.4(MYH7):c.3245+3A>T rs727505355
NM_000257.4(MYH7):c.3404T>G (p.Leu1135Arg)
NM_000257.4(MYH7):c.3830G>A (p.Arg1277Gln) rs397516195
NM_000257.4(MYH7):c.3830G>C (p.Arg1277Pro) rs397516195
NM_000257.4(MYH7):c.3834C>T (p.Ala1278=)
NM_000257.4(MYH7):c.3853+1G>A rs202031879
NM_000257.4(MYH7):c.3929A>C (p.Gln1310Pro) rs869025481
NM_000257.4(MYH7):c.475G>C (p.Asp159His) rs730880155
NM_000257.4(MYH7):c.5287G>A (p.Ala1763Thr) rs727504355
NM_000257.4(MYH7):c.532G>A (p.Gly178Arg) rs730880156
NM_000257.4(MYH7):c.536A>C (p.Glu179Ala) rs869025476
NM_000257.4(MYH7):c.5482G>A (p.Ala1828Thr) rs886050415
NM_000257.4(MYH7):c.5561C>T (p.Thr1854Met) rs372381770
NM_000257.4(MYH7):c.5603T>C (p.Val1868Ala)
NM_000257.4(MYH7):c.5786C>T (p.Thr1929Met) rs730880918
NM_000257.4(MYH7):c.652G>T (p.Asp218Tyr)
NM_000257.4(MYH7):c.733-3C>T rs765068619
NM_000257.4(MYH7):c.793A>T (p.Thr265Ser) rs730880157
NM_000257.4(MYH7):c.976G>C (p.Ala326Pro) rs372731424

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