ClinVar Miner

List of variants in gene TNNT2 reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_000364.4(TNNT2):c.144C>T (p.Thr48=) rs746492909
NM_000364.4(TNNT2):c.199+14G>A rs876657590
NM_000364.4(TNNT2):c.200-4C>G rs397516448
NM_000364.4(TNNT2):c.208A>G (p.Met70Val) rs141837529
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.295-14C>T rs747477576
NM_000364.4(TNNT2):c.412-6_412-4del rs397516462
NM_000364.4(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_000364.4(TNNT2):c.489+7dup rs397516467
NM_000364.4(TNNT2):c.52+7G>A rs374443596
NM_000364.4(TNNT2):c.567C>T (p.Ser189=) rs397516474
NM_000364.4(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_000364.4(TNNT2):c.710+13A>C rs563883763
NM_000364.4(TNNT2):c.711-4G>T rs201753429
NM_000364.4(TNNT2):c.765C>T (p.Phe255=) rs397516481
NM_000364.4(TNNT2):c.801+6C>T rs727504260
NM_000364.4(TNNT2):c.828C>T (p.Asn276=) rs376923877
NM_000364.4(TNNT2):c.90C>T (p.Asp30=) rs727503515

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