ClinVar Miner

List of variants in gene TNNT2 reported as likely pathogenic by GeneDx

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Total variants: 26
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HGVS dbSNP
NM_000364.4(TNNT2):c.259C>A (p.Pro87Thr) rs730881096
NM_000364.4(TNNT2):c.277G>A (p.Glu93Lys) rs727504244
NM_000364.4(TNNT2):c.281G>C (p.Arg94Thr) rs397516452
NM_000364.4(TNNT2):c.287A>C (p.Asp96Ala) rs397516455
NM_000364.4(TNNT2):c.349G>A (p.Glu117Lys) rs730881099
NM_000364.4(TNNT2):c.360T>G (p.Phe120Leu) rs727504331
NM_000364.4(TNNT2):c.412G>A (p.Glu138Lys) rs730881100
NM_000364.4(TNNT2):c.421C>G (p.Arg141Gly) rs74315380
NM_000364.4(TNNT2):c.445C>A (p.Arg149Ser) rs397516465
NM_000364.4(TNNT2):c.445C>T (p.Arg149Cys) rs397516465
NM_000364.4(TNNT2):c.452G>A (p.Arg151Gln) rs730881101
NM_000364.4(TNNT2):c.473G>A (p.Arg158Gln) rs730881102
NM_000364.4(TNNT2):c.506G>A (p.Arg169Gln) rs45501500
NM_000364.4(TNNT2):c.526A>G (p.Arg176Gly) rs730881104
NM_000364.4(TNNT2):c.601-1G>A rs1085307889
NM_000364.4(TNNT2):c.758A>G (p.Glu253Gly) rs730881109
NM_000364.4(TNNT2):c.766G>A (p.Asp256Asn) rs141805127
NM_000364.4(TNNT2):c.796T>C (p.Tyr266His) rs730881112
NM_000364.4(TNNT2):c.801+5G>A rs730881113
NM_000364.4(TNNT2):c.815G>A (p.Arg272Gln) rs730881125
NM_000364.4(TNNT2):c.842+5G>A rs193922620
NM_000364.4(TNNT2):c.853C>T (p.Arg285Cys) rs121964857
NM_000364.4(TNNT2):c.854G>C (p.Arg285Pro) rs397516484
NM_000364.4(TNNT2):c.857G>A (p.Gly286Glu) rs727505233
NM_000364.4(TNNT2):c.881G>A (p.Trp294Ter) rs727504247
NM_000364.4(TNNT2):c.882G>A (p.Trp294Ter) rs730881116

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