ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance for not provided

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Total variants: 46
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HGVS dbSNP
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_000364.4(TNNT2):c.245C>A (p.Pro82His) rs386352374
NM_000364.4(TNNT2):c.268C>A (p.Pro90Thr) rs397516451
NM_000364.4(TNNT2):c.599A>C (p.Lys200Thr) rs730881105
NM_000364.4(TNNT2):c.629C>A (p.Thr210Asn) rs397516476
NM_000364.4(TNNT2):c.703C>G (p.Gln235Glu) rs730881108
NM_000364.4(TNNT2):c.826A>T (p.Asn276Tyr) rs4523540
NM_000364.4(TNNT2):c.881G>T (p.Trp294Leu) rs727504247
NM_000364.4(TNNT2):c.97G>T (p.Glu33Ter) rs377474357
NM_001001430.3(TNNT2):c.40_41+1del rs1558251170
NM_001276345.2(TNNT2):c.10A>C (p.Ile4Leu) rs139705141
NM_001276345.2(TNNT2):c.208A>G (p.Met70Val) rs141837529
NM_001276345.2(TNNT2):c.236C>T (p.Ser79Leu) rs761953142
NM_001276345.2(TNNT2):c.254T>G (p.Val85Gly) rs730881095
NM_001276345.2(TNNT2):c.313A>C (p.Met105Leu) rs397516458
NM_001276345.2(TNNT2):c.41+16A>G rs370729174
NM_001276345.2(TNNT2):c.443A>G (p.Gln148Arg) rs730880232
NM_001276345.2(TNNT2):c.451del (p.Arg151fs) rs730881115
NM_001276345.2(TNNT2):c.472C>T (p.Arg158Trp) rs730881123
NM_001276345.2(TNNT2):c.490-1G>C rs111344408
NM_001276345.2(TNNT2):c.502C>G (p.Arg168Gly) rs730881103
NM_001276345.2(TNNT2):c.516_517delinsTT (p.Glu172_Glu173delinsAspTer) rs730881118
NM_001276345.2(TNNT2):c.522C>A (p.Asn174Lys) rs483352833
NM_001276345.2(TNNT2):c.550_552AAG[2] (p.Lys186del) rs1558225172
NM_001276345.2(TNNT2):c.564G>C (p.Leu188Phe) rs201270895
NM_001276345.2(TNNT2):c.601-1G>A rs483352835
NM_001276345.2(TNNT2):c.610-6C>T rs45516702
NM_001276345.2(TNNT2):c.706G>A (p.Glu236Lys) rs730881107
NM_001276345.2(TNNT2):c.752A>G (p.Tyr251Cys) rs200500421
NM_001276345.2(TNNT2):c.762G>T (p.Glu254Asp) rs45466197
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>A (p.Asp259Asn) rs141805127
NM_001276345.2(TNNT2):c.803A>T (p.Lys268Ile) rs397516482
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.823C>T (p.Arg275Ter) rs748970759
NM_001276345.2(TNNT2):c.835A>G (p.Asn279Asp) rs4523540
NM_001276345.2(TNNT2):c.837C>T (p.Asn279=) rs376923877
NM_001276345.2(TNNT2):c.852-3C>T rs749454768
NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys) rs121964857
NM_001276345.2(TNNT2):c.865G>A (p.Gly289Arg) rs757664792
NM_001276345.2(TNNT2):c.883G>A (p.Gly295Arg) rs147940106
NM_001276345.2(TNNT2):c.884G>A (p.Gly295Glu) rs1272169178
NM_001276345.2(TNNT2):c.887G>A (p.Arg296His) rs141121678

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