ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance for Cardiomyopathy

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Total variants: 148
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HGVS dbSNP gnomAD frequency
NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys) rs121964857 0.00044
NM_001276345.2(TNNT2):c.692T>C (p.Ile231Thr) rs45520032 0.00015
NM_001276345.2(TNNT2):c.762G>T (p.Glu254Asp) rs45466197 0.00007
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.248A>G (p.Asn83Ser) rs397516450 0.00004
NM_001276345.2(TNNT2):c.403G>A (p.Asp135Asn) rs765359025 0.00004
NM_001276345.2(TNNT2):c.461G>A (p.Arg154Gln) rs745632066 0.00004
NM_001276345.2(TNNT2):c.601-7G>A rs369759523 0.00004
NM_001276345.2(TNNT2):c.706G>A (p.Glu236Lys) rs730881107 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.779T>C (p.Leu260Pro) rs376037051 0.00004
NM_001276345.2(TNNT2):c.810+5G>A rs730881113 0.00004
NM_001276345.2(TNNT2):c.*3C>A rs529731863 0.00003
NM_001276345.2(TNNT2):c.103G>A (p.Glu35Lys) rs867180029 0.00003
NM_001276345.2(TNNT2):c.411+6T>A rs761043932 0.00003
NM_001276345.2(TNNT2):c.436G>A (p.Glu146Lys) rs371142225 0.00003
NM_001276345.2(TNNT2):c.460C>T (p.Arg154Trp) rs483352832 0.00003
NM_001276345.2(TNNT2):c.609+3G>A rs997358710 0.00003
NM_001276345.2(TNNT2):c.617G>A (p.Arg206Gln) rs371047521 0.00003
NM_001276345.2(TNNT2):c.691A>G (p.Ile231Val) rs886045828 0.00003
NM_001276345.2(TNNT2):c.883G>A (p.Gly295Arg) rs147940106 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.295-13G>A rs764804961 0.00002
NM_001276345.2(TNNT2):c.341C>T (p.Ala114Val) rs727504245 0.00002
NM_001276345.2(TNNT2):c.34G>A (p.Glu12Lys) rs760247765 0.00002
NM_001276345.2(TNNT2):c.40G>A (p.Glu14Lys) rs772890125 0.00002
NM_001276345.2(TNNT2):c.610-15T>A rs950076691 0.00002
NM_001276345.2(TNNT2):c.100C>A (p.Gln34Lys) rs1350800220 0.00001
NM_001276345.2(TNNT2):c.105G>T (p.Glu35Asp) rs1660031053 0.00001
NM_001276345.2(TNNT2):c.145G>A (p.Glu49Lys) rs757526942 0.00001
NM_001276345.2(TNNT2):c.172G>A (p.Glu58Lys) rs1659923363 0.00001
NM_001276345.2(TNNT2):c.200-4C>G rs397516448 0.00001
NM_001276345.2(TNNT2):c.277G>A (p.Glu93Lys) rs727504244 0.00001
NM_001276345.2(TNNT2):c.281dup (p.Val95fs) rs780087395 0.00001
NM_001276345.2(TNNT2):c.349G>A (p.Glu117Lys) rs730881099 0.00001
NM_001276345.2(TNNT2):c.411C>T (p.Ile137=) rs727504322 0.00001
NM_001276345.2(TNNT2):c.419G>A (p.Arg140His) rs1339922051 0.00001
NM_001276345.2(TNNT2):c.431G>A (p.Arg144Gln) rs754037135 0.00001
NM_001276345.2(TNNT2):c.452G>A (p.Arg151Gln) rs730881101 0.00001
NM_001276345.2(TNNT2):c.472C>T (p.Arg158Trp) rs730881123 0.00001
NM_001276345.2(TNNT2):c.487G>T (p.Ala163Ser) rs727505030 0.00001
NM_001276345.2(TNNT2):c.490-1G>C rs111344408 0.00001
NM_001276345.2(TNNT2):c.52+3A>C rs763459940 0.00001
NM_001276345.2(TNNT2):c.601-1G>A rs483352835 0.00001
NM_001276345.2(TNNT2):c.613G>A (p.Glu205Lys) rs150008205 0.00001
NM_001276345.2(TNNT2):c.659A>T (p.Lys220Met) rs190805300 0.00001
NM_001276345.2(TNNT2):c.677G>A (p.Arg226Lys) rs1205564576 0.00001
NM_001276345.2(TNNT2):c.720-9C>A rs763204242 0.00001
NM_001276345.2(TNNT2):c.752A>G (p.Tyr251Cys) rs200500421 0.00001
NM_001276345.2(TNNT2):c.775G>A (p.Asp259Asn) rs141805127 0.00001
NM_001276345.2(TNNT2):c.815A>G (p.Asn272Ser) rs397516483 0.00001
NM_001276345.2(TNNT2):c.835A>G (p.Asn279Asp) rs4523540 0.00001
NM_001276345.2(TNNT2):c.886C>T (p.Arg296Cys) rs367785431 0.00001
NM_001276345.2(TNNT2):c.*2G>A rs1449258380
NM_001276345.2(TNNT2):c.*3C>G rs529731863
NM_001276345.2(TNNT2):c.-1C>T rs776936911
NM_001276345.2(TNNT2):c.121G>A (p.Asp41Asn) rs748078123
NM_001276345.2(TNNT2):c.124G>A (p.Ala42Thr) rs1571649102
NM_001276345.2(TNNT2):c.148G>A (p.Glu50Lys) rs1660021596
NM_001276345.2(TNNT2):c.163+4A>T
NM_001276345.2(TNNT2):c.163G>T (p.Glu55Ter) rs730881120
NM_001276345.2(TNNT2):c.164-14C>A
NM_001276345.2(TNNT2):c.16G>A (p.Glu6Lys) rs2102316961
NM_001276345.2(TNNT2):c.175G>A (p.Glu59Lys) rs568628521
NM_001276345.2(TNNT2):c.193G>C (p.Ala65Pro) rs1659919080
NM_001276345.2(TNNT2):c.194C>A (p.Ala65Asp)
NM_001276345.2(TNNT2):c.199+8_199+9delinsAGCAAAGGAGGCTGAAGGAAGCAAAGGAGGCTGAAGGAAGCAAAGGAGGCTGAAGGTACC rs1659917504
NM_001276345.2(TNNT2):c.227del (p.Lys76fs) rs34008819
NM_001276345.2(TNNT2):c.229C>A (p.Pro77Thr)
NM_001276345.2(TNNT2):c.233+3G>A
NM_001276345.2(TNNT2):c.236C>G (p.Ser79Trp) rs761953142
NM_001276345.2(TNNT2):c.238T>C (p.Phe80Leu) rs886039053
NM_001276345.2(TNNT2):c.244C>G (p.Pro82Ala)
NM_001276345.2(TNNT2):c.253G>A (p.Val85Met) rs1659529300
NM_001276345.2(TNNT2):c.268C>A (p.Pro90Thr) rs397516451
NM_001276345.2(TNNT2):c.268C>T (p.Pro90Ser) rs397516451
NM_001276345.2(TNNT2):c.271G>A (p.Asp91Asn) rs1571630555
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.282_283del (p.Arg94fs) rs1259701355
NM_001276345.2(TNNT2):c.294+5G>A rs533357783
NM_001276345.2(TNNT2):c.295-1G>C
NM_001276345.2(TNNT2):c.295-3C>A rs1659453460
NM_001276345.2(TNNT2):c.300C>G (p.Ile100Met) rs1230932782
NM_001276345.2(TNNT2):c.304_305insTTC (p.His101_Arg102insLeu) rs730881117
NM_001276345.2(TNNT2):c.313A>G (p.Met105Val) rs397516458
NM_001276345.2(TNNT2):c.316G>A (p.Glu106Lys) rs869312881
NM_001276345.2(TNNT2):c.329A>G (p.Asn110Ser) rs727505027
NM_001276345.2(TNNT2):c.347_348delinsCT (p.Ile116Thr) rs1553282523
NM_001276345.2(TNNT2):c.374A>T (p.Lys125Ile) rs1558230900
NM_001276345.2(TNNT2):c.375del (p.Glu126fs) rs560019679
NM_001276345.2(TNNT2):c.395C>A (p.Ser132Tyr) rs1659426786
NM_001276345.2(TNNT2):c.406A>T (p.Arg136Trp) rs786204405
NM_001276345.2(TNNT2):c.408G>C (p.Arg136Ser) rs2102260528
NM_001276345.2(TNNT2):c.427G>C (p.Glu143Gln) rs1316344347
NM_001276345.2(TNNT2):c.430C>T (p.Arg144Trp) rs45525839
NM_001276345.2(TNNT2):c.443A>G (p.Gln148Arg) rs730880232
NM_001276345.2(TNNT2):c.451del (p.Arg151fs) rs730881115
NM_001276345.2(TNNT2):c.481C>T (p.Arg161Cys) rs45608937
NM_001276345.2(TNNT2):c.489+5G>A rs1659249392
NM_001276345.2(TNNT2):c.490-14C>G
NM_001276345.2(TNNT2):c.4T>C (p.Ser2Pro) rs765584396
NM_001276345.2(TNNT2):c.506G>A (p.Arg169Gln) rs45501500
NM_001276345.2(TNNT2):c.511G>A (p.Glu171Lys) rs1659064618
NM_001276345.2(TNNT2):c.53-11_53-10del rs764129741
NM_001276345.2(TNNT2):c.550AAG[2] (p.Lys186del) rs1558225172
NM_001276345.2(TNNT2):c.552G>C (p.Lys184Asn) rs566113559
NM_001276345.2(TNNT2):c.552G>T (p.Lys184Asn) rs566113559
NM_001276345.2(TNNT2):c.564G>C (p.Leu188Phe) rs201270895
NM_001276345.2(TNNT2):c.569A>G (p.Asn190Ser)
NM_001276345.2(TNNT2):c.572T>C (p.Met191Thr) rs869025538
NM_001276345.2(TNNT2):c.584G>A (p.Gly195Glu) rs1558224822
NM_001276345.2(TNNT2):c.5C>T (p.Ser2Phe) rs981844273
NM_001276345.2(TNNT2):c.601-8C>A rs397516475
NM_001276345.2(TNNT2):c.610-10C>T rs375547142
NM_001276345.2(TNNT2):c.610-7C>A rs1658744962
NM_001276345.2(TNNT2):c.611C>T (p.Thr204Ile) rs2102235172
NM_001276345.2(TNNT2):c.634C>T (p.Gln212Ter)
NM_001276345.2(TNNT2):c.662T>G (p.Ile221Ser)
NM_001276345.2(TNNT2):c.679A>T (p.Lys227Ter) rs397516478
NM_001276345.2(TNNT2):c.682G>C (p.Val228Leu) rs397516479
NM_001276345.2(TNNT2):c.682G>T (p.Val228Leu) rs397516479
NM_001276345.2(TNNT2):c.709G>C (p.Asp237His) rs867035950
NM_001276345.2(TNNT2):c.719+12_719+28del
NM_001276345.2(TNNT2):c.719+3G>T rs111451787
NM_001276345.2(TNNT2):c.719+5G>A rs1658715625
NM_001276345.2(TNNT2):c.719G>A (p.Arg240Lys) rs2102233852
NM_001276345.2(TNNT2):c.720-32_720-14dup
NM_001276345.2(TNNT2):c.720-6_720-3del rs1658597866
NM_001276345.2(TNNT2):c.727G>A (p.Ala243Thr) rs1658594625
NM_001276345.2(TNNT2):c.751T>C (p.Tyr251His) rs1571600689
NM_001276345.2(TNNT2):c.764C>T (p.Ala255Val) rs369181536
NM_001276345.2(TNNT2):c.772T>C (p.Phe258Leu) rs730881110
NM_001276345.2(TNNT2):c.772T>G (p.Phe258Val) rs730881110
NM_001276345.2(TNNT2):c.775G>T (p.Asp259Tyr)
NM_001276345.2(TNNT2):c.776A>T (p.Asp259Val)
NM_001276345.2(TNNT2):c.782A>G (p.Gln261Arg) rs2102228802
NM_001276345.2(TNNT2):c.811-13A>C
NM_001276345.2(TNNT2):c.811-1G>T rs1658235582
NM_001276345.2(TNNT2):c.812T>G (p.Ile271Ser) rs371384395
NM_001276345.2(TNNT2):c.824G>A (p.Arg275Gln) rs730881125
NM_001276345.2(TNNT2):c.851+5G>A rs193922620
NM_001276345.2(TNNT2):c.870G>T (p.Lys290Asn) rs752111672
NM_001276345.2(TNNT2):c.98-4C>G rs775895925

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