ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 74
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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.208A>G (p.Met70Val) rs141837529 0.00009
NM_001276345.2(TNNT2):c.762G>T (p.Glu254Asp) rs45466197 0.00007
NM_001276345.2(TNNT2):c.887G>A (p.Arg296His) rs141121678 0.00005
NM_001276345.2(TNNT2):c.10A>C (p.Ile4Leu) rs139705141 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.706G>A (p.Glu236Lys) rs730881107 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.883G>A (p.Gly295Arg) rs147940106 0.00003
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.391G>A (p.Val131Ile) rs537067344 0.00002
NM_001276345.2(TNNT2):c.136G>C (p.Ala46Pro) rs397516447 0.00001
NM_001276345.2(TNNT2):c.254T>G (p.Val85Gly) rs730881095 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.404A>T (p.Asp135Val) rs759758840 0.00001
NM_001276345.2(TNNT2):c.412G>A (p.Glu138Lys) rs730881100 0.00001
NM_001276345.2(TNNT2):c.472C>T (p.Arg158Trp) rs730881123 0.00001
NM_001276345.2(TNNT2):c.473G>A (p.Arg158Gln) rs730881102 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.601-1G>A rs483352835 0.00001
NM_001276345.2(TNNT2):c.775G>A (p.Asp259Asn) rs141805127 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.97G>T (p.Glu33Ter) rs377474357 0.00001
NM_001276345.2(TNNT2):c.238T>C (p.Phe80Leu) rs886039053
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.281G>C (p.Arg94Thr) rs397516452
NM_001276345.2(TNNT2):c.301C>T (p.His101Tyr) rs2102262282
NM_001276345.2(TNNT2):c.304_305insTTC (p.His101_Arg102insLeu) rs730881117
NM_001276345.2(TNNT2):c.307A>G (p.Lys103Glu) rs730881122
NM_001276345.2(TNNT2):c.319_321del (p.Lys107del) rs2102261838
NM_001276345.2(TNNT2):c.333G>C (p.Glu111Asp) rs1659441464
NM_001276345.2(TNNT2):c.347_348delinsCT (p.Ile116Thr) rs1553282523
NM_001276345.2(TNNT2):c.349G>T (p.Glu117Ter) rs730881099
NM_001276345.2(TNNT2):c.397C>G (p.Leu133Val) rs2102260733
NM_001276345.2(TNNT2):c.41+3_41+6del
NM_001276345.2(TNNT2):c.418C>G (p.Arg140Gly) rs397516463
NM_001276345.2(TNNT2):c.443A>G (p.Gln148Arg) rs730880232
NM_001276345.2(TNNT2):c.451del (p.Arg151fs) rs730881115
NM_001276345.2(TNNT2):c.496A>G (p.Arg166Gly) rs2102245950
NM_001276345.2(TNNT2):c.498G>T (p.Arg166Ser)
NM_001276345.2(TNNT2):c.502C>G (p.Arg168Gly) rs730881103
NM_001276345.2(TNNT2):c.506G>A (p.Arg169Gln) rs45501500
NM_001276345.2(TNNT2):c.522C>A (p.Asn174Lys) rs483352833
NM_001276345.2(TNNT2):c.529A>G (p.Lys177Glu) rs2102245349
NM_001276345.2(TNNT2):c.593T>C (p.Ile198Thr) rs878854148
NM_001276345.2(TNNT2):c.599A>C (p.Lys200Thr) rs730881105
NM_001276345.2(TNNT2):c.614A>G (p.Glu205Gly) rs1658740460
NM_001276345.2(TNNT2):c.667G>C (p.Ala223Pro) rs1057518606
NM_001276345.2(TNNT2):c.712C>G (p.Gln238Glu) rs730881108
NM_001276345.2(TNNT2):c.716T>C (p.Leu239Pro) rs2102233867
NM_001276345.2(TNNT2):c.719+1G>C rs1169197265
NM_001276345.2(TNNT2):c.764C>T (p.Ala255Val) rs369181536
NM_001276345.2(TNNT2):c.767A>G (p.Glu256Gly) rs730881109
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.781C>A (p.Gln261Lys) rs730881111
NM_001276345.2(TNNT2):c.805T>C (p.Tyr269His) rs730881112
NM_001276345.2(TNNT2):c.806A>G (p.Tyr269Cys) rs1553280112
NM_001276345.2(TNNT2):c.808G>A (p.Glu270Lys) rs1131691898
NM_001276345.2(TNNT2):c.824G>A (p.Arg275Gln) rs730881125
NM_001276345.2(TNNT2):c.835A>T (p.Asn279Tyr) rs4523540
NM_001276345.2(TNNT2):c.842A>T (p.Asn281Ile) rs863225119
NM_001276345.2(TNNT2):c.852-1G>T rs730881114
NM_001276345.2(TNNT2):c.865G>A (p.Gly289Arg) rs757664792
NM_001276345.2(TNNT2):c.866G>A (p.Gly289Glu) rs727505233
NM_001276345.2(TNNT2):c.890G>T (p.Trp297Leu) rs727504247
NM_001276345.2(TNNT2):c.94G>C (p.Asp32His)

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