ClinVar Miner

List of variants in gene TNNT2 reported as likely pathogenic

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Gene type:
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Total variants: 70
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HGVS dbSNP
NC_000001.11:g.201359651G>A
NM_000364.4(TNNT2):c.259C>A (p.Pro87Thr) rs730881096
NM_000364.4(TNNT2):c.268C>T (p.Pro90Ser) rs397516451
NM_000364.4(TNNT2):c.274G>A (p.Gly92Arg) rs727504255
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.294T>G (p.Asp98Glu) rs397516454
NM_000364.4(TNNT2):c.305G>A (p.Arg102Gln) rs121964856
NM_000364.4(TNNT2):c.307A>C (p.Lys103Gln) rs730881122
NM_000364.4(TNNT2):c.310C>T (p.Arg104Cys) rs727503513
NM_000364.4(TNNT2):c.311G>A (p.Arg104His) rs397516457
NM_000364.4(TNNT2):c.311G>T (p.Arg104Leu) rs397516457
NM_000364.4(TNNT2):c.316_318del (p.Glu106del) rs727504277
NM_000364.4(TNNT2):c.321G>T (p.Lys107Asn) rs397516459
NM_000364.4(TNNT2):c.341C>T (p.Ala114Val) rs727504245
NM_000364.4(TNNT2):c.349G>A (p.Glu117Lys) rs730881099
NM_000364.4(TNNT2):c.354_355delinsGT (p.His119Tyr) rs876658027
NM_000364.4(TNNT2):c.358T>C (p.Phe120Leu) rs121964858
NM_000364.4(TNNT2):c.360T>G (p.Phe120Leu) rs727504331
NM_000364.4(TNNT2):c.382G>A (p.Glu128Lys) rs397516461
NM_000364.4(TNNT2):c.385G>C (p.Glu129Gln)
NM_000364.4(TNNT2):c.3G>A (p.Met1Ile) rs1289914935
NM_000364.4(TNNT2):c.412G>A (p.Glu138Lys) rs730881100
NM_000364.4(TNNT2):c.418C>T (p.Arg140Cys) rs397516463
NM_000364.4(TNNT2):c.421C>G (p.Arg141Gly) rs74315380
NM_000364.4(TNNT2):c.421C>T (p.Arg141Trp) rs74315380
NM_000364.4(TNNT2):c.422G>C (p.Arg141Pro) rs397516464
NM_000364.4(TNNT2):c.430C>G (p.Arg144Gly) rs45525839
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.446G>A (p.Arg149His) rs397516466
NM_000364.4(TNNT2):c.451del (p.Arg151fs) rs730881115
NM_000364.4(TNNT2):c.452G>A (p.Arg151Gln) rs730881101
NM_000364.4(TNNT2):c.460C>T (p.Arg154Trp) rs483352832
NM_000364.4(TNNT2):c.473G>A (p.Arg158Gln) rs730881102
NM_000364.4(TNNT2):c.490-1G>C rs111344408
NM_000364.4(TNNT2):c.506G>A (p.Arg169Gln) rs45501500
NM_000364.4(TNNT2):c.517G>A (p.Glu173Lys) rs1558225569
NM_000364.4(TNNT2):c.526A>G (p.Arg176Gly) rs730881104
NM_000364.4(TNNT2):c.544G>T (p.Ala182Ser) rs730881097
NM_000364.4(TNNT2):c.547C>T (p.Arg183Trp) rs727503512
NM_000364.4(TNNT2):c.548G>A (p.Arg183Gln) rs397516471
NM_000364.4(TNNT2):c.566C>T (p.Ser189Phe) rs727504246
NM_000364.4(TNNT2):c.601-1G>A rs1085307889
NM_000364.4(TNNT2):c.601-363del
NM_000364.4(TNNT2):c.601-373G>A rs483352835
NM_000364.4(TNNT2):c.634C>T (p.Arg212Trp) rs45586240
NM_000364.4(TNNT2):c.635G>A (p.Arg212Gln) rs121964860
NM_000364.4(TNNT2):c.653T>C (p.Ile218Thr) rs863225120
NM_000364.4(TNNT2):c.710+2T>A
NM_000364.4(TNNT2):c.755C>T (p.Ala252Val) rs369181536
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.775G>A (p.Glu259Lys) rs727504488
NM_000364.4(TNNT2):c.794A>T (p.Lys265Ile) rs397516482
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.828C>A (p.Asn276Lys) rs376923877
NM_000364.4(TNNT2):c.833A>T (p.Asn278Ile) rs863225119
NM_000364.4(TNNT2):c.842+1G>C rs111377893
NM_000364.4(TNNT2):c.842+1G>T rs111377893
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.878G>A (p.Arg293His) rs141121678
NM_000364.4(TNNT2):c.881G>A (p.Trp294Ter) rs727504247
NM_000364.4(TNNT2):c.882G>A (p.Trp294Ter) rs730881116

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