ClinVar Miner

List of variants in gene TNNT2 reported as uncertain significance by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

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Total variants: 24
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HGVS dbSNP
NM_001001430.2(TNNT2):c.580-45_580-20delins275
NM_001276345.2(TNNT2):c.-1C>T rs776936911
NM_001276345.2(TNNT2):c.172G>A (p.Glu58Lys)
NM_001276345.2(TNNT2):c.175G>A (p.Glu59Lys) rs568628521
NM_001276345.2(TNNT2):c.200-4C>G rs397516448
NM_001276345.2(TNNT2):c.282A>T (p.Arg94Ser) rs397516453
NM_001276345.2(TNNT2):c.300C>G (p.Ile100Met)
NM_001276345.2(TNNT2):c.341C>T (p.Ala114Val) rs727504245
NM_001276345.2(TNNT2):c.406A>T (p.Arg136Trp)
NM_001276345.2(TNNT2):c.411+6T>A rs761043932
NM_001276345.2(TNNT2):c.452G>A (p.Arg151Gln) rs730881101
NM_001276345.2(TNNT2):c.552G>C (p.Lys184Asn) rs566113559
NM_001276345.2(TNNT2):c.552G>T (p.Lys184Asn) rs566113559
NM_001276345.2(TNNT2):c.572T>C (p.Met191Thr) rs869025538
NM_001276345.2(TNNT2):c.584G>A (p.Gly195Glu) rs1558224822
NM_001276345.2(TNNT2):c.610-10C>T rs375547142
NM_001276345.2(TNNT2):c.719+5G>A
NM_001276345.2(TNNT2):c.720-6_720-3del
NM_001276345.2(TNNT2):c.762G>T (p.Glu254Asp) rs45466197
NM_001276345.2(TNNT2):c.803A>T (p.Lys268Ile) rs397516482
NM_001276345.2(TNNT2):c.810+5G>A rs730881113
NM_001276345.2(TNNT2):c.835A>G (p.Asn279Asp) rs4523540
NM_001276345.2(TNNT2):c.851+5G>A rs193922620
NM_001276345.2(TNNT2):c.98-4C>G rs775895925

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