ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance by Center for Human Genetics,University of Leuven

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Total variants: 11
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HGVS dbSNP
NM_000257.4(MYH7):c.1128C>A (p.Asp376Glu) rs2231126
NM_000257.4(MYH7):c.1331A>G (p.Asn444Ser) rs730880159
NM_000257.4(MYH7):c.1351C>G (p.Gln451Glu) rs730880871
NM_000257.4(MYH7):c.2047G>C (p.Val683Leu) rs1566532876
NM_000257.4(MYH7):c.3169G>A (p.Gly1057Ser) rs397516179
NM_000257.4(MYH7):c.3382G>A (p.Ala1128Thr) rs199552354
NM_000257.4(MYH7):c.3637G>A (p.Val1213Met) rs397516182
NM_000257.4(MYH7):c.4145G>A (p.Arg1382Gln) rs727504325
NM_000257.4(MYH7):c.5287G>A (p.Ala1763Thr) rs727504355
NM_000257.4(MYH7):c.5471A>G (p.Asn1824Ser) rs760218400
NM_000257.4(MYH7):c.976G>C (p.Ala326Pro) rs372731424

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