ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 122
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HGVS dbSNP
NC_000001.11:g.201359651G>A
NC_000001.11:g.201365610A>T
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_000364.4(TNNT2):c.136G>C (p.Ala46Pro) rs397516447
NM_000364.4(TNNT2):c.144C>T (p.Thr48=) rs746492909
NM_000364.4(TNNT2):c.163+12G>A rs45580032
NM_000364.4(TNNT2):c.163+5G>A rs727504254
NM_000364.4(TNNT2):c.199+14G>A rs876657590
NM_000364.4(TNNT2):c.200-11A>G rs368658464
NM_000364.4(TNNT2):c.200-4C>G rs397516448
NM_000364.4(TNNT2):c.208A>C (p.Met70Leu) rs141837529
NM_000364.4(TNNT2):c.208A>G (p.Met70Val) rs141837529
NM_000364.4(TNNT2):c.228G>C (p.Lys76Asn) rs727504869
NM_000364.4(TNNT2):c.233+6T>C rs397516449
NM_000364.4(TNNT2):c.237G>A (p.Ser79=) rs3729845
NM_000364.4(TNNT2):c.248A>G (p.Asn83Ser) rs397516450
NM_000364.4(TNNT2):c.260C>T (p.Pro87Leu) rs144900708
NM_000364.4(TNNT2):c.266T>A (p.Ile89Asn) rs121964855
NM_000364.4(TNNT2):c.268C>T (p.Pro90Ser) rs397516451
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.274G>A (p.Gly92Arg) rs727504255
NM_000364.4(TNNT2):c.277G>A (p.Glu93Lys) rs727504244
NM_000364.4(TNNT2):c.279G>C (p.Glu93Asp) rs727503514
NM_000364.4(TNNT2):c.281G>C (p.Arg94Thr) rs397516452
NM_000364.4(TNNT2):c.282A>T (p.Arg94Ser) rs397516453
NM_000364.4(TNNT2):c.287A>C (p.Asp96Ala) rs397516455
NM_000364.4(TNNT2):c.294+7G>A rs45490292
NM_000364.4(TNNT2):c.294T>G (p.Asp98Glu) rs397516454
NM_000364.4(TNNT2):c.295-14C>T rs747477576
NM_000364.4(TNNT2):c.304C>T (p.Arg102Trp) rs397516456
NM_000364.4(TNNT2):c.305G>A (p.Arg102Gln) rs121964856
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.313A>G (p.Met105Val) rs397516458
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.329A>G (p.Asn110Ser) rs727505027
NM_000364.4(TNNT2):c.341C>T (p.Ala114Val) rs727504245
NM_000364.4(TNNT2):c.348C>T (p.Ile116=) rs3729547
NM_000364.4(TNNT2):c.354_355delinsGT (p.His119Tyr) rs876658027
NM_000364.4(TNNT2):c.355C>T (p.His119Tyr) rs397516460
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.39G>A (p.Glu13=) rs727503516
NM_000364.4(TNNT2):c.411C>T (p.Ile137=) rs727504322
NM_000364.4(TNNT2):c.412-6_412-4del rs397516462
NM_000364.4(TNNT2):c.418C>T (p.Arg140Cys) rs397516463
NM_000364.4(TNNT2):c.421C>T (p.Arg141Trp) rs74315380
NM_000364.4(TNNT2):c.422G>A (p.Arg141Gln) rs397516464
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>T (p.Arg149Cys) rs397516465
NM_000364.4(TNNT2):c.446G>A (p.Arg149His) rs397516466
NM_000364.4(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_000364.4(TNNT2):c.451C>T (p.Arg151Trp) rs74315379
NM_000364.4(TNNT2):c.460C>T (p.Arg154Trp) rs483352832
NM_000364.4(TNNT2):c.474G>C (p.Arg158=) rs35914325
NM_000364.4(TNNT2):c.487G>A (p.Ala163Thr) rs727505030
NM_000364.4(TNNT2):c.489+7dup rs397516467
NM_000364.4(TNNT2):c.503G>A (p.Arg168Gln) rs397516468
NM_000364.4(TNNT2):c.505C>T (p.Arg169Ter) rs397516469
NM_000364.4(TNNT2):c.506G>A (p.Arg169Gln) rs45501500
NM_000364.4(TNNT2):c.508_510GAG[3] (p.Glu173del) rs397516470
NM_000364.4(TNNT2):c.52+6C>T rs397516472
NM_000364.4(TNNT2):c.52+7G>A rs374443596
NM_000364.4(TNNT2):c.522C>T (p.Asn174=) rs483352833
NM_000364.4(TNNT2):c.53-11_53-7del rs45533739
NM_000364.4(TNNT2):c.544G>T (p.Ala182Ser) rs730881097
NM_000364.4(TNNT2):c.547C>G (p.Arg183Gly) rs727503512
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.560C>A (p.Ala187Asp) rs397516473
NM_000364.4(TNNT2):c.564G>C (p.Leu188Phe) rs201270895
NM_000364.4(TNNT2):c.566C>T (p.Ser189Phe) rs727504246
NM_000364.4(TNNT2):c.567C>T (p.Ser189=) rs397516474
NM_000364.4(TNNT2):c.573G>T (p.Met191Ile) rs876658028
NM_000364.4(TNNT2):c.581T>C (p.Phe194Ser) rs1553281172
NM_000364.4(TNNT2):c.601-373G>A rs483352835
NM_000364.4(TNNT2):c.601-379G>A rs369759523
NM_000364.4(TNNT2):c.601-380C>A rs397516475
NM_000364.4(TNNT2):c.601-380C>T rs397516475
NM_000364.4(TNNT2):c.619A>G (p.Lys207Glu) rs727503511
NM_000364.4(TNNT2):c.629C>T (p.Thr210Ile) rs397516476
NM_000364.4(TNNT2):c.635G>A (p.Arg212Gln) rs121964860
NM_000364.4(TNNT2):c.635G>C (p.Arg212Pro) rs121964860
NM_000364.4(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_000364.4(TNNT2):c.641_643AGA[3] (p.Lys217del) rs45578238
NM_000364.4(TNNT2):c.670A>G (p.Lys224Glu) rs397516478
NM_000364.4(TNNT2):c.673G>T (p.Val225Leu) rs397516479
NM_000364.4(TNNT2):c.68-5_68-3delinsTT rs397516362
NM_000364.4(TNNT2):c.68-8A>G rs115805892
NM_000364.4(TNNT2):c.683T>C (p.Ile228Thr) rs45520032
NM_000364.4(TNNT2):c.710+13A>C rs563883763
NM_000364.4(TNNT2):c.711-13_711-11del rs397516480
NM_000364.4(TNNT2):c.711-4G>T rs201753429
NM_000364.4(TNNT2):c.711-6G>A rs113471285
NM_000364.4(TNNT2):c.711-7C>T rs376303087
NM_000364.4(TNNT2):c.753G>T (p.Glu251Asp) rs45466197
NM_000364.4(TNNT2):c.755C>T (p.Ala252Val) rs369181536
NM_000364.4(TNNT2):c.765C>T (p.Phe255=) rs397516481
NM_000364.4(TNNT2):c.775G>A (p.Glu259Lys) rs727504488
NM_000364.4(TNNT2):c.779A>G (p.Lys260Arg) rs3730238
NM_000364.4(TNNT2):c.794A>T (p.Lys265Ile) rs397516482
NM_000364.4(TNNT2):c.801+6C>T rs727504260
NM_000364.4(TNNT2):c.806A>G (p.Asn269Ser) rs397516483
NM_000364.4(TNNT2):c.828C>A (p.Asn276Lys) rs376923877
NM_000364.4(TNNT2):c.828C>T (p.Asn276=) rs376923877
NM_000364.4(TNNT2):c.842+1G>A rs111377893
NM_000364.4(TNNT2):c.842+1G>T rs111377893
NM_000364.4(TNNT2):c.845C>A (p.Ser282Tyr) rs876658029
NM_000364.4(TNNT2):c.853C>T (p.Arg285Cys) rs121964857
NM_000364.4(TNNT2):c.854G>A (p.Arg285His) rs397516484
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.877C>T (p.Arg293Cys) rs367785431
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
NM_000364.4(TNNT2):c.90C>T (p.Asp30=) rs727503515
NM_000364.4(TNNT2):c.97G>A (p.Glu33Lys) rs377474357

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