ClinVar Miner

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

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Total variants: 41
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HGVS dbSNP
NM_000364.4(TNNT2):c.10A>C (p.Ile4Leu) rs139705141
NM_000364.4(TNNT2):c.208A>G (p.Met70Val) rs141837529
NM_000364.4(TNNT2):c.245C>A (p.Pro82His) rs386352374
NM_000364.4(TNNT2):c.254T>G (p.Val85Gly) rs730881095
NM_000364.4(TNNT2):c.268C>A (p.Pro90Thr) rs397516451
NM_000364.4(TNNT2):c.41+16A>G rs370729174
NM_000364.4(TNNT2):c.441G>A (p.Gln147=) rs1044313920
NM_000364.4(TNNT2):c.443A>G (p.Gln148Arg) rs730880232
NM_000364.4(TNNT2):c.451del (p.Arg151fs) rs730881115
NM_000364.4(TNNT2):c.472C>T (p.Arg158Trp) rs730881123
NM_000364.4(TNNT2):c.490-1G>C rs111344408
NM_000364.4(TNNT2):c.502C>G (p.Arg168Gly) rs730881103
NM_000364.4(TNNT2):c.516_517delinsTT (p.Glu172_Glu173delinsAspTer) rs730881118
NM_000364.4(TNNT2):c.522C>A (p.Asn174Lys) rs483352833
NM_000364.4(TNNT2):c.564G>C (p.Leu188Phe) rs201270895
NM_000364.4(TNNT2):c.599A>C (p.Lys200Thr) rs730881105
NM_000364.4(TNNT2):c.601-373G>A rs483352835
NM_000364.4(TNNT2):c.601-6C>T rs45516702
NM_000364.4(TNNT2):c.629C>A (p.Thr210Asn) rs397516476
NM_000364.4(TNNT2):c.697G>A (p.Glu233Lys) rs730881107
NM_000364.4(TNNT2):c.703C>G (p.Gln235Glu) rs730881108
NM_000364.4(TNNT2):c.743A>G (p.Tyr248Cys) rs200500421
NM_000364.4(TNNT2):c.753G>T (p.Glu251Asp) rs45466197
NM_000364.4(TNNT2):c.755C>T (p.Ala252Val) rs369181536
NM_000364.4(TNNT2):c.763T>C (p.Phe255Leu) rs730881110
NM_000364.4(TNNT2):c.763T>G (p.Phe255Val) rs730881110
NM_000364.4(TNNT2):c.766G>A (p.Asp256Asn) rs141805127
NM_000364.4(TNNT2):c.794A>T (p.Lys265Ile) rs397516482
NM_000364.4(TNNT2):c.797A>G (p.Tyr266Cys) rs1553280112
NM_000364.4(TNNT2):c.799G>A (p.Glu267Lys) rs1131691898
NM_000364.4(TNNT2):c.826A>G (p.Asn276Asp) rs4523540
NM_000364.4(TNNT2):c.826A>T (p.Asn276Tyr) rs4523540
NM_000364.4(TNNT2):c.828C>T (p.Asn276=) rs376923877
NM_000364.4(TNNT2):c.853C>T (p.Arg285Cys) rs121964857
NM_000364.4(TNNT2):c.856G>A (p.Gly286Arg) rs757664792
NM_000364.4(TNNT2):c.874G>A (p.Gly292Arg) rs147940106
NM_000364.4(TNNT2):c.875G>A (p.Gly292Glu) rs1272169178
NM_000364.4(TNNT2):c.878G>A (p.Arg293His) rs141121678
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

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