ClinVar Miner

List of variants in gene TNNT2 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP gnomAD frequency
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.-14-201G>A rs45535342 0.01244
NM_001276345.2(TNNT2):c.489+119G>A rs139924149 0.01113
NM_001276345.2(TNNT2):c.490-127C>T rs3730236 0.01107
NM_001276345.2(TNNT2):c.601-298del rs140190878 0.01106
NM_001276345.2(TNNT2):c.67+321G>C rs114576011 0.01103
NM_001276345.2(TNNT2):c.851+43C>T rs45570832 0.01103
NM_001276345.2(TNNT2):c.720-71C>T rs140139755 0.01071
NM_001276345.2(TNNT2):c.294+7G>A rs45490292 0.01066
NM_001276345.2(TNNT2):c.810+65G>A rs45517846 0.01064
NM_001276345.2(TNNT2):c.810+136C>T rs114141823 0.01062
NM_001276345.2(TNNT2):c.67+97C>T rs45514004 0.01060
NM_001276345.2(TNNT2):c.41+75C>G rs10920185 0.00978
NM_001276345.2(TNNT2):c.489+57G>C rs45527945 0.00942
NM_001276345.2(TNNT2):c.68-8A>G rs115805892 0.00864
NM_001276345.2(TNNT2):c.489+265A>G rs146087349 0.00479
NM_001276345.2(TNNT2):c.811-233G>A rs45521432 0.00447
NM_001276345.2(TNNT2):c.42-96C>T rs45586136 0.00404
NM_001276345.2(TNNT2):c.490-101A>G rs45516299 0.00399
NM_001276345.2(TNNT2):c.164-57A>C rs45560244 0.00394
NM_001276345.2(TNNT2):c.67+189T>C rs150991558 0.00394
NM_001276345.2(TNNT2):c.53-47C>G rs45553832 0.00345
NM_001276345.2(TNNT2):c.810+27G>C rs142475266 0.00203
NM_001276345.2(TNNT2):c.41+41C>T rs45548233 0.00119
NM_001276345.2(TNNT2):c.98-81G>A rs45576939 0.00067
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249 0.00046
NM_001276345.2(TNNT2):c.41+16A>G rs370729174 0.00029
NM_001276345.2(TNNT2):c.200-11A>G rs368658464 0.00021
NM_001276345.2(TNNT2):c.-49C>T rs1050772817 0.00017
NM_001276345.2(TNNT2):c.852-23A>G rs371692788 0.00010
NM_001276345.2(TNNT2):c.208A>G (p.Met70Val) rs141837529 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.114G>A (p.Ala38=) rs200283086 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.52+13G>A rs376820377 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.*3C>A rs529731863 0.00003
NM_001276345.2(TNNT2):c.435C>T (p.Ala145=) rs375675827 0.00003
NM_001276345.2(TNNT2):c.601-6G>A rs760197357 0.00003
NM_001276345.2(TNNT2):c.282A>G (p.Arg94=) rs397516453 0.00002
NM_001276345.2(TNNT2):c.63T>G (p.Val21=) rs397516477 0.00002
NM_001276345.2(TNNT2):c.-3A>G rs752977897 0.00001
NM_001276345.2(TNNT2):c.144C>T (p.Thr48=) rs746492909 0.00001
NM_001276345.2(TNNT2):c.153C>G (p.Thr51=) rs1347127737 0.00001
NM_001276345.2(TNNT2):c.33C>T (p.Tyr11=) rs148027842 0.00001
NM_001276345.2(TNNT2):c.450C>T (p.Ile150=) rs200604266 0.00001
NM_001276345.2(TNNT2):c.861C>A (p.Thr287=) rs754211195 0.00001
NM_001276345.2(TNNT2):c.-43C>T rs1571707151
NM_001276345.2(TNNT2):c.234-10T>C rs1342160801
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.342G>A (p.Ala114=) rs918054429
NM_001276345.2(TNNT2):c.41+6dup rs1479180367
NM_001276345.2(TNNT2):c.412-94del rs35559054
NM_001276345.2(TNNT2):c.42-6T>C rs1660720268
NM_001276345.2(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_001276345.2(TNNT2):c.490-11C>T rs770704074
NM_001276345.2(TNNT2):c.68-3C>T rs587780970
NM_001276345.2(TNNT2):c.68-5del rs2102295381
NM_001276345.2(TNNT2):c.68-70G>T rs12049476
NM_001276345.2(TNNT2):c.777C>T (p.Asp259=) rs2102228925
NM_001276345.2(TNNT2):c.810+64C>G rs45496994
NM_001276345.2(TNNT2):c.810+64C>T
NM_001276345.2(TNNT2):c.810+7C>A rs373069229

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