ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance for not specified

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Gene type:
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Total variants: 69
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HGVS dbSNP
NC_000001.11:g.201365610A>T
NM_000364.4(TNNT2):c.110C>G (p.Ala37Gly)
NM_000364.4(TNNT2):c.136G>C (p.Ala46Pro) rs397516447
NM_000364.4(TNNT2):c.163+5G>A rs727504254
NM_000364.4(TNNT2):c.200-11A>G rs368658464
NM_000364.4(TNNT2):c.208A>C (p.Met70Leu) 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.248A>G (p.Asn83Ser) rs397516450
NM_000364.4(TNNT2):c.260C>T (p.Pro87Leu) rs144900708
NM_000364.4(TNNT2):c.268C>T (p.Pro90Ser) rs397516451
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.313A>G (p.Met105Val) rs397516458
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.347_348delinsCT (p.Ile116Thr) rs1553282523
NM_000364.4(TNNT2):c.355C>T (p.His119Tyr) rs397516460
NM_000364.4(TNNT2):c.358T>G (p.Phe120Val) rs121964858
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.445C>T (p.Arg149Cys) rs397516465
NM_000364.4(TNNT2):c.446G>A (p.Arg149His) rs397516466
NM_000364.4(TNNT2):c.487G>A (p.Ala163Thr) rs727505030
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.516_517delinsTT (p.Glu172_Glu173delinsAspTer) rs730881118
NM_000364.4(TNNT2):c.52+6C>T rs397516472
NM_000364.4(TNNT2):c.547C>G (p.Arg183Gly) rs727503512
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.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.658G>C (p.Ala220Pro) rs1057518606
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.683T>C (p.Ile228Thr) rs45520032
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.772C>A (p.Gln258Lys) rs730881111
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.806A>G (p.Asn269Ser) rs397516483
NM_000364.4(TNNT2):c.842+5G>A rs193922620
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.97G>A (p.Glu33Lys) rs377474357
NM_001001430.2(TNNT2):c.580-45_580-20delins275

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