ClinVar Miner

List of variants in gene TNNI3 reported as uncertain significance for Cardiovascular phenotype

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Total variants: 118
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HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702 0.00006
NM_000363.5(TNNI3):c.282+5C>G rs770260866 0.00004
NM_000363.5(TNNI3):c.292C>T (p.Arg98Ter) rs730881068 0.00004
NM_000363.5(TNNI3):c.293G>A (p.Arg98Gln) rs747522089 0.00004
NM_000363.5(TNNI3):c.308G>A (p.Arg103His) rs371000425 0.00004
NM_000363.5(TNNI3):c.556C>T (p.Arg186Trp) rs760978512 0.00004
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872 0.00003
NM_000363.5(TNNI3):c.167T>C (p.Ile56Thr) rs545441942 0.00002
NM_000363.5(TNNI3):c.236G>T (p.Arg79Leu) rs397516342 0.00002
NM_000363.5(TNNI3):c.92C>T (p.Thr31Met) rs201928445 0.00002
NM_000363.5(TNNI3):c.143A>C (p.Gln48Pro) rs200720341 0.00001
NM_000363.5(TNNI3):c.146dup (p.Lys50fs) rs1162696593 0.00001
NM_000363.5(TNNI3):c.164A>C (p.Gln55Pro) rs775512887 0.00001
NM_000363.5(TNNI3):c.220C>T (p.Arg74Cys) rs375795196 0.00001
NM_000363.5(TNNI3):c.232A>T (p.Thr78Ser) rs786204399 0.00001
NM_000363.5(TNNI3):c.250G>T (p.Glu84Ter) rs759523214 0.00001
NM_000363.5(TNNI3):c.278T>C (p.Leu93Pro) rs776035548 0.00001
NM_000363.5(TNNI3):c.307C>T (p.Arg103Cys) rs397516344 0.00001
NM_000363.5(TNNI3):c.322G>A (p.Asp108Asn) rs766958196 0.00001
NM_000363.5(TNNI3):c.331A>G (p.Arg111Gly) rs730881088 0.00001
NM_000363.5(TNNI3):c.341T>C (p.Ile114Thr) rs762692450 0.00001
NM_000363.5(TNNI3):c.347C>G (p.Ala116Gly) rs777177571 0.00001
NM_000363.5(TNNI3):c.34C>T (p.Pro12Ser) rs553214254 0.00001
NM_000363.5(TNNI3):c.35C>T (p.Pro12Leu) rs768052584 0.00001
NM_000363.5(TNNI3):c.368C>T (p.Thr123Met) rs397516345 0.00001
NM_000363.5(TNNI3):c.384G>A (p.Leu128=) rs373130533 0.00001
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp) rs730881071 0.00001
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn) rs397516348 0.00001
NM_000363.5(TNNI3):c.482C>T (p.Ala161Val) rs753413305 0.00001
NM_000363.5(TNNI3):c.5C>T (p.Ala2Val) rs397516359 0.00001
NM_000363.5(TNNI3):c.604G>C (p.Glu202Gln) rs1470970097 0.00001
NM_000363.5(TNNI3):c.620A>G (p.Lys207Arg) rs367672692 0.00001
NM_000363.5(TNNI3):c.629G>A (p.Ser210Asn) rs1240826681 0.00001
NM_000363.5(TNNI3):c.632G>T (p.Ter211Leu) rs730881084 0.00001
NM_000363.5(TNNI3):c.104C>T (p.Ala35Val) rs1190447904
NM_000363.5(TNNI3):c.108+5G>A rs1261858318
NM_000363.5(TNNI3):c.11+4A>G rs2515505147
NM_000363.5(TNNI3):c.114A>T (p.Lys38Asn) rs730881066
NM_000363.5(TNNI3):c.115T>C (p.Ser39Pro) rs1568859416
NM_000363.5(TNNI3):c.119A>T (p.Lys40Met) rs2515502447
NM_000363.5(TNNI3):c.125C>T (p.Ser42Phe) rs2085732640
NM_000363.5(TNNI3):c.127G>T (p.Ala43Ser) rs727505023
NM_000363.5(TNNI3):c.130T>A (p.Ser44Thr) rs2147285302
NM_000363.5(TNNI3):c.131C>G (p.Ser44Trp) rs730881085
NM_000363.5(TNNI3):c.131C>T (p.Ser44Leu) rs730881085
NM_000363.5(TNNI3):c.134G>A (p.Arg45Lys) rs2147285293
NM_000363.5(TNNI3):c.13A>G (p.Ser5Gly) rs2085740955
NM_000363.5(TNNI3):c.146T>A (p.Leu49Gln) rs1397663689
NM_000363.5(TNNI3):c.150G>A (p.Lys50=) rs730881086
NM_000363.5(TNNI3):c.151A>G (p.Thr51Ala) rs2515501787
NM_000363.5(TNNI3):c.173A>G (p.Lys58Arg) rs878853955
NM_000363.5(TNNI3):c.178G>C (p.Glu60Gln)
NM_000363.5(TNNI3):c.190G>C (p.Glu64Gln) rs1245885836
NM_000363.5(TNNI3):c.194C>T (p.Ala65Val) rs1057518784
NM_000363.5(TNNI3):c.197A>G (p.Glu66Gly) rs1047163086
NM_000363.5(TNNI3):c.198G>T (p.Glu66Asp)
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.220C>A (p.Arg74Ser) rs375795196
NM_000363.5(TNNI3):c.220C>G (p.Arg74Gly) rs375795196
NM_000363.5(TNNI3):c.221G>C (p.Arg74Pro) rs886039022
NM_000363.5(TNNI3):c.227T>C (p.Leu76Pro) rs1443859469
NM_000363.5(TNNI3):c.229A>T (p.Ser77Cys) rs2515501630
NM_000363.5(TNNI3):c.248T>C (p.Leu83Pro)
NM_000363.5(TNNI3):c.258del (p.Leu88fs) rs727503507
NM_000363.5(TNNI3):c.269T>G (p.Phe90Cys) rs2515501535
NM_000363.5(TNNI3):c.26C>G (p.Ala9Gly)
NM_000363.5(TNNI3):c.303C>A (p.His101Gln)
NM_000363.5(TNNI3):c.318G>C (p.Lys106Asn) rs750350912
NM_000363.5(TNNI3):c.335dup (p.Tyr112Ter) rs1568858517
NM_000363.5(TNNI3):c.337G>A (p.Asp113Asn) rs779064799
NM_000363.5(TNNI3):c.356C>T (p.Thr119Ile) rs184709702
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506
NM_000363.5(TNNI3):c.372+2T>A rs1319124481
NM_000363.5(TNNI3):c.372+4G>C rs1285163191
NM_000363.5(TNNI3):c.373A>T (p.Ile125Phe) rs1599909309
NM_000363.5(TNNI3):c.380A>G (p.Asp127Gly) rs1384750266
NM_000363.5(TNNI3):c.382C>G (p.Leu128Val) rs2515498630
NM_000363.5(TNNI3):c.393G>A (p.Lys131=) rs2515498605
NM_000363.5(TNNI3):c.403C>A (p.Leu135Ile) rs1555863549
NM_000363.5(TNNI3):c.403C>T (p.Leu135Phe) rs1555863549
NM_000363.5(TNNI3):c.406C>G (p.Arg136Gly) rs1393946566
NM_000363.5(TNNI3):c.406C>T (p.Arg136Ter) rs1393946566
NM_000363.5(TNNI3):c.410G>A (p.Gly137Asp) rs2515498564
NM_000363.5(TNNI3):c.421C>G (p.Arg141Gly) rs730881071
NM_000363.5(TNNI3):c.451G>A (p.Ala151Thr) rs730881072
NM_000363.5(TNNI3):c.492G>T (p.Lys164Asn)
NM_000363.5(TNNI3):c.497C>A (p.Ser166Tyr) rs727504242
NM_000363.5(TNNI3):c.497C>G (p.Ser166Cys) rs727504242
NM_000363.5(TNNI3):c.502G>A (p.Asp168Asn) rs1085308019
NM_000363.5(TNNI3):c.503A>G (p.Asp168Gly)
NM_000363.5(TNNI3):c.511G>A (p.Ala171Thr) rs121917761
NM_000363.5(TNNI3):c.534G>T (p.Lys178Asn) rs1394531956
NM_000363.5(TNNI3):c.538G>A (p.Asp180Asn) rs1060503103
NM_000363.5(TNNI3):c.539A>G (p.Asp180Gly) rs1060499912
NM_000363.5(TNNI3):c.547_548delinsGT (p.Lys183Val) rs2515498208
NM_000363.5(TNNI3):c.549+4_549+7del rs2515498193
NM_000363.5(TNNI3):c.554A>G (p.Asn185Ser) rs730881079
NM_000363.5(TNNI3):c.55A>C (p.Ile19Leu) rs755862334
NM_000363.5(TNNI3):c.560A>C (p.Glu187Ala)
NM_000363.5(TNNI3):c.562G>A (p.Val188Met) rs193922409
NM_000363.5(TNNI3):c.566G>C (p.Gly189Ala) rs587782980
NM_000363.5(TNNI3):c.577A>G (p.Lys193Glu) rs730881080
NM_000363.5(TNNI3):c.581A>C (p.Asn194Thr) rs730881081
NM_000363.5(TNNI3):c.583A>C (p.Ile195Leu) rs876658024
NM_000363.5(TNNI3):c.586G>T (p.Asp196Tyr) rs104894727
NM_000363.5(TNNI3):c.587A>G (p.Asp196Gly) rs2147281695
NM_000363.5(TNNI3):c.599G>A (p.Gly200Glu) rs878853957
NM_000363.5(TNNI3):c.601A>G (p.Met201Val)
NM_000363.5(TNNI3):c.602T>C (p.Met201Thr) rs727504365
NM_000363.5(TNNI3):c.605A>G (p.Glu202Gly) rs2515495746
NM_000363.5(TNNI3):c.614A>C (p.Lys205Thr) rs1555862962
NM_000363.5(TNNI3):c.626A>C (p.Glu209Ala) rs730881083
NM_000363.5(TNNI3):c.79C>G (p.Arg27Gly) rs1555864366
NM_000363.5(TNNI3):c.79C>T (p.Arg27Cys) rs1555864366
NM_000363.5(TNNI3):c.80G>C (p.Arg27Pro) rs2147285955
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr) rs796104366
NM_000363.5(TNNI3):c.95A>G (p.Glu32Gly) rs2515503663
NM_000363.5(TNNI3):c.9T>A (p.Asp3Glu) rs2085744143

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