ClinVar Miner

List of variants in gene TNNT2 reported as likely benign for Familial hypertrophic cardiomyopathy 2; Left ventricular noncompaction 6; Familial restrictive cardiomyopathy 3

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Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_000364.4(TNNT2):c.114G>A (p.Ala38=) rs200283086
NM_000364.4(TNNT2):c.144C>T (p.Thr48=) rs746492909
NM_000364.4(TNNT2):c.255G>A (p.Val85=) rs780115529
NM_000364.4(TNNT2):c.270C>G (p.Pro90=) rs140245123
NM_000364.4(TNNT2):c.270C>T (p.Pro90=) rs140245123
NM_000364.4(TNNT2):c.273T>C (p.Asp91=) rs763782935
NM_000364.4(TNNT2):c.285G>A (p.Val95=) rs1060503885
NM_000364.4(TNNT2):c.390C>T (p.Leu130=) rs758543857
NM_000364.4(TNNT2):c.459G>A (p.Glu153=) rs775274966
NM_000364.4(TNNT2):c.489+9C>A rs1060503884
NM_000364.4(TNNT2):c.498G>A (p.Arg166=) rs750399630
NM_000364.4(TNNT2):c.567C>T (p.Ser189=) rs397516474
NM_000364.4(TNNT2):c.601-10C>T rs375547142
NM_000364.4(TNNT2):c.601-378G>A rs760197357
NM_000364.4(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_000364.4(TNNT2):c.711-4G>T rs201753429
NM_000364.4(TNNT2):c.711-6G>A rs113471285
NM_000364.4(TNNT2):c.765C>T (p.Phe255=) rs397516481
NM_000364.4(TNNT2):c.769C>T (p.Leu257=) rs977853063
NM_000364.4(TNNT2):c.802-4G>A rs1431082504
NM_000364.4(TNNT2):c.819C>T (p.Asn273=) rs1553279337
NM_000364.4(TNNT2):c.84A>G (p.Arg28=) rs370895664
NM_000364.4(TNNT2):c.852C>A (p.Thr284=) rs754211195
NM_000364.4(TNNT2):c.873C>T (p.Thr291=) rs45465693
NM_000364.4(TNNT2):c.96C>T (p.Asp32=) rs751728017
NM_000364.4(TNNT2):c.98-81G>A rs45576939

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