ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 122
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HGVS dbSNP gnomAD frequency
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.10A>C (p.Ile4Leu) rs139705141 0.00004
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.706G>A (p.Glu236Lys) rs730881107 0.00004
NM_001276345.2(TNNT2):c.779T>C (p.Leu260Pro) rs376037051 0.00004
NM_001276345.2(TNNT2):c.103G>A (p.Glu35Lys) rs867180029 0.00003
NM_001276345.2(TNNT2):c.436G>A (p.Glu146Lys) rs371142225 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.721G>C (p.Glu241Gln) rs1189945246 0.00003
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.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.-3A>G rs752977897 0.00001
NM_001276345.2(TNNT2):c.145G>A (p.Glu49Lys) rs757526942 0.00001
NM_001276345.2(TNNT2):c.163+1G>T rs113051005 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.349G>A (p.Glu117Lys) rs730881099 0.00001
NM_001276345.2(TNNT2):c.404A>T (p.Asp135Val) rs759758840 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.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.505C>T (p.Arg169Ter) rs397516469 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.677G>A (p.Arg226Lys) rs1205564576 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.803A>T (p.Lys268Ile) rs397516482 0.00001
NM_001276345.2(TNNT2):c.823C>T (p.Arg275Ter) rs748970759 0.00001
NM_001276345.2(TNNT2):c.835A>G (p.Asn279Asp) rs4523540 0.00001
NM_001276345.2(TNNT2):c.-1C>A rs776936911
NM_001276345.2(TNNT2):c.-1C>T rs776936911
NM_001276345.2(TNNT2):c.104A>T (p.Glu35Val)
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.131C>T (p.Ala44Val)
NM_001276345.2(TNNT2):c.142A>G (p.Thr48Ala)
NM_001276345.2(TNNT2):c.155G>A (p.Arg52Lys)
NM_001276345.2(TNNT2):c.157G>A (p.Ala53Thr)
NM_001276345.2(TNNT2):c.163+2T>C
NM_001276345.2(TNNT2):c.163G>A (p.Glu55Lys) rs730881120
NM_001276345.2(TNNT2):c.175G>A (p.Glu59Lys) rs568628521
NM_001276345.2(TNNT2):c.209T>A (p.Met70Lys)
NM_001276345.2(TNNT2):c.238T>C (p.Phe80Leu) rs886039053
NM_001276345.2(TNNT2):c.248A>C (p.Asn83Thr)
NM_001276345.2(TNNT2):c.262A>G (p.Lys88Glu) rs1659525886
NM_001276345.2(TNNT2):c.268C>T (p.Pro90Ser) rs397516451
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.294+4A>C
NM_001276345.2(TNNT2):c.294+5G>A rs533357783
NM_001276345.2(TNNT2):c.295-1G>A rs113876817
NM_001276345.2(TNNT2):c.298A>G (p.Ile100Val)
NM_001276345.2(TNNT2):c.301C>T (p.His101Tyr) rs2102262282
NM_001276345.2(TNNT2):c.309G>T (p.Lys103Asn) rs778426227
NM_001276345.2(TNNT2):c.324C>A (p.Asp108Glu) rs1553282545
NM_001276345.2(TNNT2):c.332A>G (p.Glu111Gly)
NM_001276345.2(TNNT2):c.341C>A (p.Ala114Glu) rs727504245
NM_001276345.2(TNNT2):c.347_348delinsCT (p.Ile116Thr) rs1553282523
NM_001276345.2(TNNT2):c.352G>T (p.Ala118Ser)
NM_001276345.2(TNNT2):c.355C>T (p.His119Tyr) rs397516460
NM_001276345.2(TNNT2):c.375del (p.Glu126fs) rs560019679
NM_001276345.2(TNNT2):c.388C>G (p.Leu130Val)
NM_001276345.2(TNNT2):c.3G>A (p.Met1Ile) rs1289914935
NM_001276345.2(TNNT2):c.404A>G (p.Asp135Gly)
NM_001276345.2(TNNT2):c.408G>C (p.Arg136Ser) rs2102260528
NM_001276345.2(TNNT2):c.412G>C (p.Glu138Gln)
NM_001276345.2(TNNT2):c.413A>G (p.Glu138Gly)
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.445C>T (p.Arg149Cys) rs397516465
NM_001276345.2(TNNT2):c.446G>T (p.Arg149Leu)
NM_001276345.2(TNNT2):c.448A>G (p.Ile150Val)
NM_001276345.2(TNNT2):c.451del (p.Arg151fs) rs730881115
NM_001276345.2(TNNT2):c.463G>A (p.Glu155Lys) rs984218824
NM_001276345.2(TNNT2):c.469G>A (p.Glu157Lys)
NM_001276345.2(TNNT2):c.470A>G (p.Glu157Gly)
NM_001276345.2(TNNT2):c.481C>T (p.Arg161Cys) rs45608937
NM_001276345.2(TNNT2):c.482G>T (p.Arg161Leu)
NM_001276345.2(TNNT2):c.499G>T (p.Ala167Ser) rs1553281319
NM_001276345.2(TNNT2):c.4T>C (p.Ser2Pro) rs765584396
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.517G>A (p.Glu173Lys) rs1558225569
NM_001276345.2(TNNT2):c.52+4A>G
NM_001276345.2(TNNT2):c.552G>T (p.Lys184Asn) rs566113559
NM_001276345.2(TNNT2):c.554A>G (p.Lys185Arg)
NM_001276345.2(TNNT2):c.569_571dup (p.Asn190_Met191insAsn)
NM_001276345.2(TNNT2):c.580T>C (p.Phe194Leu)
NM_001276345.2(TNNT2):c.583G>C (p.Gly195Arg)
NM_001276345.2(TNNT2):c.583G>T (p.Gly195Trp)
NM_001276345.2(TNNT2):c.609+1G>C
NM_001276345.2(TNNT2):c.611C>T (p.Thr204Ile) rs2102235172
NM_001276345.2(TNNT2):c.614_615del (p.Glu205fs) rs760664767
NM_001276345.2(TNNT2):c.616C>T (p.Arg206Trp) rs730881106
NM_001276345.2(TNNT2):c.620A>G (p.Lys207Arg)
NM_001276345.2(TNNT2):c.632G>A (p.Arg211Lys)
NM_001276345.2(TNNT2):c.643C>T (p.Arg215Trp) rs45586240
NM_001276345.2(TNNT2):c.67+5G>A
NM_001276345.2(TNNT2):c.719+1G>T
NM_001276345.2(TNNT2):c.719+3G>C
NM_001276345.2(TNNT2):c.719+3G>T rs111451787
NM_001276345.2(TNNT2):c.719G>A (p.Arg240Lys) rs2102233852
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.806A>G (p.Tyr269Cys) rs1553280112
NM_001276345.2(TNNT2):c.820C>A (p.Leu274Ile)
NM_001276345.2(TNNT2):c.838G>A (p.Asp280Asn) rs121964861
NM_001276345.2(TNNT2):c.842A>T (p.Asn281Ile) rs863225119
NM_001276345.2(TNNT2):c.844C>T (p.Gln282Ter) rs796925245
NM_001276345.2(TNNT2):c.852-2A>C rs111692981
NM_001276345.2(TNNT2):c.886C>A (p.Arg296Ser) rs367785431
NM_001276345.2(TNNT2):c.895T>C (p.Ter299Gln)

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