ClinVar Miner

List of variants in gene MYH7 reported as uncertain significance by CSER_CC_NCGL; University of Washington Medical Center

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Gene type:
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Total variants: 17
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HGVS dbSNP
NM_000257.3(MYH7):c.115G>A (p.Val39Met) rs376160714
NM_000257.3(MYH7):c.2183C>T (p.Ala728Val) rs121913644
NM_000257.3(MYH7):c.2359C>T (p.Arg787Cys) rs145677314
NM_000257.3(MYH7):c.3301G>A (p.Gly1101Ser) rs367546859
NM_000257.3(MYH7):c.4052C>T (p.Thr1351Met) rs370403289
NM_000257.3(MYH7):c.5305C>A (p.Leu1769Met) rs139222507
NM_000257.3(MYH7):c.5494C>T (p.Arg1832Cys) rs201865159
NM_000257.3(MYH7):c.5536C>T (p.Arg1846Cys) rs12590294
NM_000257.3(MYH7):c.5561C>T (p.Thr1854Met) rs372381770
NM_000257.3(MYH7):c.958G>A (p.Val320Met) rs376897125
NM_000257.3(MYH7):c.976G>C (p.Ala326Pro) rs372731424
NM_000257.4(MYH7):c.2360G>A (p.Arg787His) rs376754645
NM_000257.4(MYH7):c.2608C>T (p.Arg870Cys) rs138049878
NM_000257.4(MYH7):c.2945T>C (p.Met982Thr) rs145532615
NM_000257.4(MYH7):c.3981C>A (p.Asn1327Lys) rs141764279
NM_000257.4(MYH7):c.4258C>T (p.Arg1420Trp) rs145213771
NM_000257.4(MYH7):c.77C>T (p.Ala26Val) rs186964570

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