ClinVar Miner

List of variants in gene MYBPC3 reported as uncertain significance by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute

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Total variants: 20
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HGVS dbSNP
NM_000256.3(MYBPC3):c.1112C>G (p.Pro371Arg) rs397515887
NM_000256.3(MYBPC3):c.1227-13G>A rs397515893
NM_000256.3(MYBPC3):c.1466A>T (p.Asp489Val) rs1555122204
NM_000256.3(MYBPC3):c.1721G>A (p.Arg574Gln) rs397515922
NM_000256.3(MYBPC3):c.1828G>C (p.Asp610His) rs371564200
NM_000256.3(MYBPC3):c.1859G>T (p.Gly620Val) rs730880556
NM_000256.3(MYBPC3):c.1934C>T (p.Pro645Leu) rs397515938
NM_000256.3(MYBPC3):c.2063C>T (p.Thr688Met) rs3729946
NM_000256.3(MYBPC3):c.2560A>G (p.Met854Val) rs373171036
NM_000256.3(MYBPC3):c.3065G>C (p.Arg1022Pro) rs397516000
NM_000256.3(MYBPC3):c.317C>G (p.Pro106Arg) rs986848670
NM_000256.3(MYBPC3):c.3326C>A (p.Thr1109Asn) rs397516016
NM_000256.3(MYBPC3):c.3407_3409delACT (p.Tyr1136del) rs730880674
NM_000256.3(MYBPC3):c.3535G>A (p.Glu1179Lys) rs199669878
NM_000256.3(MYBPC3):c.373G>T (p.Ala125Ser) rs370958401
NM_000256.3(MYBPC3):c.3742G>A (p.Gly1248Arg) rs202147520
NM_000256.3(MYBPC3):c.436A>C (p.Thr146Pro) rs397516048
NM_000256.3(MYBPC3):c.479G>A (p.Arg160Gln) rs730880617
NM_000256.3(MYBPC3):c.646G>A (p.Ala216Thr) rs201098973
NM_000256.3(MYBPC3):c.961G>A (p.Val321Met) rs200119454

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