ClinVar Miner

List of variants in gene TNNT2 studied for not specified

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Gene type:
ClinVar version:
Total variants: 148
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HGVS dbSNP gnomAD frequency
NM_001276345.2(TNNT2):c.601-32A>C rs1104859 0.73965
NM_001276345.2(TNNT2):c.348C>T (p.Ile116=) rs3729547 0.69444
NM_001276345.2(TNNT2):c.811-122C>G rs45509695 0.22049
NM_001276345.2(TNNT2):c.811-33C>T rs2275863 0.22049
NM_001276345.2(TNNT2):c.237G>A (p.Ser79=) rs3729845 0.08311
NM_001276345.2(TNNT2):c.788A>G (p.Lys263Arg) rs3730238 0.05965
NM_001276345.2(TNNT2):c.610-90G>A rs11810834 0.03251
NM_001276345.2(TNNT2):c.163+12G>A rs45580032 0.01441
NM_001276345.2(TNNT2):c.851+22C>T rs45495692 0.01327
NM_001276345.2(TNNT2):c.42-20G>A rs45561443 0.01192
NM_001276345.2(TNNT2):c.294+7G>A rs45490292 0.01066
NM_001276345.2(TNNT2):c.68-8A>G rs115805892 0.00864
NM_001276345.2(TNNT2):c.610-81C>T rs28730745 0.00831
NM_001276345.2(TNNT2):c.474G>C (p.Arg158=) rs35914325 0.00788
NM_001276345.2(TNNT2):c.200-29C>G rs45449197 0.00690
NM_001276345.2(TNNT2):c.52+48G>A rs45582534 0.00432
NM_001276345.2(TNNT2):c.68-3del rs200153031 0.00133
NM_001276345.2(TNNT2):c.68-5C>T rs540630390 0.00133
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249 0.00046
NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys) rs121964857 0.00044
NM_001276345.2(TNNT2):c.720-13_720-11del rs397516480 0.00031
NM_001276345.2(TNNT2):c.200-11A>G rs368658464 0.00021
NM_001276345.2(TNNT2):c.692T>C (p.Ile231Thr) rs45520032 0.00015
NM_001276345.2(TNNT2):c.852-19C>T rs759855940 0.00011
NM_001276345.2(TNNT2):c.208A>G (p.Met70Val) rs141837529 0.00009
NM_001276345.2(TNNT2):c.295-19C>T rs587780969 0.00009
NM_001276345.2(TNNT2):c.720-4G>T rs201753429 0.00009
NM_001276345.2(TNNT2):c.774C>T (p.Phe258=) rs397516481 0.00009
NM_001276345.2(TNNT2):c.837C>T (p.Asn279=) rs376923877 0.00009
NM_001276345.2(TNNT2):c.52+7G>A rs374443596 0.00007
NM_001276345.2(TNNT2):c.762G>T (p.Glu254Asp) rs45466197 0.00007
NM_001276345.2(TNNT2):c.-15+6G>T rs778890563 0.00006
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=) rs200283086 0.00006
NM_001276345.2(TNNT2):c.295-14C>T rs747477576 0.00006
NM_001276345.2(TNNT2):c.489+18C>T rs377743847 0.00006
NM_001276345.2(TNNT2):c.601-8C>T rs397516475 0.00006
NM_001276345.2(TNNT2):c.90C>T (p.Asp30=) rs727503515 0.00006
NM_001276345.2(TNNT2):c.567C>T (p.Ser189=) rs397516474 0.00005
NM_001276345.2(TNNT2):c.863G>A (p.Arg288His) rs397516484 0.00005
NM_001276345.2(TNNT2):c.887G>A (p.Arg296His) rs141121678 0.00005
NM_001276345.2(TNNT2):c.-15+10G>A rs754752990 0.00004
NM_001276345.2(TNNT2):c.248A>G (p.Asn83Ser) rs397516450 0.00004
NM_001276345.2(TNNT2):c.52+13G>A rs376820377 0.00004
NM_001276345.2(TNNT2):c.601-7G>A rs369759523 0.00004
NM_001276345.2(TNNT2):c.720-5T>G rs730881092 0.00004
NM_001276345.2(TNNT2):c.720-7C>T rs376303087 0.00004
NM_001276345.2(TNNT2):c.882C>T (p.Thr294=) rs45465693 0.00004
NM_001276345.2(TNNT2):c.42-29C>T rs886038366 0.00003
NM_001276345.2(TNNT2):c.435C>T (p.Ala145=) rs375675827 0.00003
NM_001276345.2(TNNT2):c.460C>T (p.Arg154Trp) rs483352832 0.00003
NM_001276345.2(TNNT2):c.552G>A (p.Lys184=) rs566113559 0.00003
NM_001276345.2(TNNT2):c.810+6C>T rs727504260 0.00003
NM_001276345.2(TNNT2):c.96C>T (p.Asp32=) rs751728017 0.00003
NM_001276345.2(TNNT2):c.110C>G (p.Ala37Gly) rs776406819 0.00002
NM_001276345.2(TNNT2):c.260C>T (p.Pro87Leu) rs144900708 0.00002
NM_001276345.2(TNNT2):c.282A>G (p.Arg94=) rs397516453 0.00002
NM_001276345.2(TNNT2):c.341C>T (p.Ala114Val) rs727504245 0.00002
NM_001276345.2(TNNT2):c.40G>A (p.Glu14Lys) rs772890125 0.00002
NM_001276345.2(TNNT2):c.52+17G>A rs776357102 0.00002
NM_001276345.2(TNNT2):c.63T>G (p.Val21=) rs397516477 0.00002
NM_001276345.2(TNNT2):c.720-6G>A rs113471285 0.00002
NM_001276345.2(TNNT2):c.-15+17G>A rs924166432 0.00001
NM_001276345.2(TNNT2):c.-40G>T rs921078883 0.00001
NM_001276345.2(TNNT2):c.136G>C (p.Ala46Pro) rs397516447 0.00001
NM_001276345.2(TNNT2):c.144C>T (p.Thr48=) rs746492909 0.00001
NM_001276345.2(TNNT2):c.163+13T>C rs527486692 0.00001
NM_001276345.2(TNNT2):c.192G>A (p.Glu64=) rs1180516886 0.00001
NM_001276345.2(TNNT2):c.200-4C>G rs397516448 0.00001
NM_001276345.2(TNNT2):c.21G>T (p.Val7=) rs777128825 0.00001
NM_001276345.2(TNNT2):c.233+6T>C rs397516449 0.00001
NM_001276345.2(TNNT2):c.254T>G (p.Val85Gly) rs730881095 0.00001
NM_001276345.2(TNNT2):c.277G>A (p.Glu93Lys) rs727504244 0.00001
NM_001276345.2(TNNT2):c.39G>A (p.Glu13=) rs727503516 0.00001
NM_001276345.2(TNNT2):c.411C>T (p.Ile137=) rs727504322 0.00001
NM_001276345.2(TNNT2):c.450C>T (p.Ile150=) rs200604266 0.00001
NM_001276345.2(TNNT2):c.505C>T (p.Arg169Ter) rs397516469 0.00001
NM_001276345.2(TNNT2):c.52+6C>T rs397516472 0.00001
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=) rs483352833 0.00001
NM_001276345.2(TNNT2):c.600+4G>A rs372988386 0.00001
NM_001276345.2(TNNT2):c.601-1G>A rs483352835 0.00001
NM_001276345.2(TNNT2):c.803A>T (p.Lys268Ile) rs397516482 0.00001
NM_001276345.2(TNNT2):c.815A>G (p.Asn272Ser) rs397516483 0.00001
NM_001276345.2(TNNT2):c.852-18G>A rs778928540 0.00001
NM_001276345.2(TNNT2):c.886C>T (p.Arg296Cys) rs367785431 0.00001
NM_000364.4(TNNT2):c.489+7dup rs397516467
NM_001001430.2(TNNT2):c.580-45_580-20delins275
NM_001001430.3(TNNT2):c.68-1623_68-1621delinsTT rs397516362
NM_001276345.2(TNNT2):c.-5A>G rs730881093
NM_001276345.2(TNNT2):c.163+12G>T rs45580032
NM_001276345.2(TNNT2):c.163+5G>A rs727504254
NM_001276345.2(TNNT2):c.164-50G>A rs3729843
NM_001276345.2(TNNT2):c.199+14G>A rs876657590
NM_001276345.2(TNNT2):c.1A>G (p.Met1Val) rs1228403814
NM_001276345.2(TNNT2):c.208A>C (p.Met70Leu) rs141837529
NM_001276345.2(TNNT2):c.228G>C (p.Lys76Asn) rs727504869
NM_001276345.2(TNNT2):c.268C>T (p.Pro90Ser) rs397516451
NM_001276345.2(TNNT2):c.270C>G (p.Pro90=) rs140245123
NM_001276345.2(TNNT2):c.270C>T (p.Pro90=) rs140245123
NM_001276345.2(TNNT2):c.279G>C (p.Glu93Asp) rs727503514
NM_001276345.2(TNNT2):c.281G>C (p.Arg94Thr) rs397516452
NM_001276345.2(TNNT2):c.282A>T (p.Arg94Ser) rs397516453
NM_001276345.2(TNNT2):c.313A>G (p.Met105Val) rs397516458
NM_001276345.2(TNNT2):c.321G>T (p.Lys107Asn) rs397516459
NM_001276345.2(TNNT2):c.329A>G (p.Asn110Ser) rs727505027
NM_001276345.2(TNNT2):c.355C>T (p.His119Tyr) rs397516460
NM_001276345.2(TNNT2):c.358T>G (p.Phe120Val) rs121964858
NM_001276345.2(TNNT2):c.412-4T>G rs757304775
NM_001276345.2(TNNT2):c.412-6_412-4del rs397516462
NM_001276345.2(TNNT2):c.441G>A (p.Gln147=) rs1044313920
NM_001276345.2(TNNT2):c.445C>T (p.Arg149Cys) rs397516465
NM_001276345.2(TNNT2):c.446G>A (p.Arg149His) rs397516466
NM_001276345.2(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_001276345.2(TNNT2):c.481C>T (p.Arg161Cys) rs45608937
NM_001276345.2(TNNT2):c.487G>A (p.Ala163Thr) rs727505030
NM_001276345.2(TNNT2):c.503G>A (p.Arg168Gln) rs397516468
NM_001276345.2(TNNT2):c.506G>A (p.Arg169Gln) rs45501500
NM_001276345.2(TNNT2):c.516_517delinsTT (p.Glu172_Glu173delinsAspTer) rs730881118
NM_001276345.2(TNNT2):c.53-11_53-7del rs45533739
NM_001276345.2(TNNT2):c.53-6G>A rs764862951
NM_001276345.2(TNNT2):c.547C>G (p.Arg183Gly) rs727503512
NM_001276345.2(TNNT2):c.560C>A (p.Ala187Asp) rs397516473
NM_001276345.2(TNNT2):c.564G>C (p.Leu188Phe) rs201270895
NM_001276345.2(TNNT2):c.573G>T (p.Met191Ile) rs876658028
NM_001276345.2(TNNT2):c.581T>C (p.Phe194Ser) rs1553281172
NM_001276345.2(TNNT2):c.592A>G (p.Ile198Val) rs730881124
NM_001276345.2(TNNT2):c.601-8C>A rs397516475
NM_001276345.2(TNNT2):c.609+15C>T rs1057523597
NM_001276345.2(TNNT2):c.628A>G (p.Lys210Glu) rs727503511
NM_001276345.2(TNNT2):c.638C>T (p.Thr213Ile) rs397516476
NM_001276345.2(TNNT2):c.643C>A (p.Arg215=) rs45586240
NM_001276345.2(TNNT2):c.644G>A (p.Arg215Gln) rs121964860
NM_001276345.2(TNNT2):c.644G>C (p.Arg215Pro) rs121964860
NM_001276345.2(TNNT2):c.667G>C (p.Ala223Pro) rs1057518606
NM_001276345.2(TNNT2):c.679A>G (p.Lys227Glu) rs397516478
NM_001276345.2(TNNT2):c.68-3C>T rs587780970
NM_001276345.2(TNNT2):c.682G>T (p.Val228Leu) rs397516479
NM_001276345.2(TNNT2):c.719+13A>C rs563883763
NM_001276345.2(TNNT2):c.764C>T (p.Ala255Val) rs369181536
NM_001276345.2(TNNT2):c.777C>T (p.Asp259=) rs2102228925
NM_001276345.2(TNNT2):c.781C>A (p.Gln261Lys) rs730881111
NM_001276345.2(TNNT2):c.784G>A (p.Glu262Lys) rs727504488
NM_001276345.2(TNNT2):c.811-19C>G rs1057522713
NM_001276345.2(TNNT2):c.842A>T (p.Asn281Ile) rs863225119
NM_001276345.2(TNNT2):c.851+5G>A rs193922620
NM_001276345.2(TNNT2):c.854C>A (p.Ser285Tyr) rs876658029
NM_001276345.2(TNNT2):c.863G>C (p.Arg288Pro) rs397516484
NM_001276345.2(TNNT2):c.866G>A (p.Gly289Glu) rs727505233
NM_001276345.2(TNNT2):c.97G>A (p.Glu33Lys) rs377474357

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