ClinVar Miner

List of variants in gene TNNT2 studied for Cardiomyopathy

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Total variants: 49
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HGVS dbSNP
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val) rs200754249
NM_000364.4(TNNT2):c.-1C>T rs776936911
NM_000364.4(TNNT2):c.175G>A (p.Glu59Lys) rs568628521
NM_000364.4(TNNT2):c.200-11A>G rs368658464
NM_000364.4(TNNT2):c.200-4C>G rs397516448
NM_000364.4(TNNT2):c.237G>A (p.Ser79=) rs3729845
NM_000364.4(TNNT2):c.304_305insTTC (p.Arg102_Lys103insLeu) rs730881117
NM_000364.4(TNNT2):c.348C>T (p.Ile116=) rs3729547
NM_000364.4(TNNT2):c.369G>A (p.Arg123=) rs1558230929
NM_000364.4(TNNT2):c.374A>T (p.Lys125Ile) rs1558230900
NM_000364.4(TNNT2):c.411+6T>A rs761043932
NM_000364.4(TNNT2):c.412-6_412-4del rs397516462
NM_000364.4(TNNT2):c.443A>G (p.Gln148Arg) rs730880232
NM_000364.4(TNNT2):c.451C>A (p.Arg151=) rs74315379
NM_000364.4(TNNT2):c.452G>A (p.Arg151Gln) rs730881101
NM_000364.4(TNNT2):c.460C>T (p.Arg154Trp) rs483352832
NM_000364.4(TNNT2):c.474G>C (p.Arg158=) rs35914325
NM_000364.4(TNNT2):c.52+7G>A rs374443596
NM_000364.4(TNNT2):c.522C>T (p.Asn174=) rs483352833
NM_000364.4(TNNT2):c.53-11_53-10del rs764129741
NM_000364.4(TNNT2):c.53-11_53-7del rs45533739
NM_000364.4(TNNT2):c.53-12del rs730881094
NM_000364.4(TNNT2):c.552G>C (p.Lys184Asn) rs566113559
NM_000364.4(TNNT2):c.552G>T (p.Lys184Asn) rs566113559
NM_000364.4(TNNT2):c.572T>C (p.Met191Thr) rs869025538
NM_000364.4(TNNT2):c.584G>A (p.Gly195Glu) rs1558224822
NM_000364.4(TNNT2):c.601-10C>T rs375547142
NM_000364.4(TNNT2):c.601-90G>A rs11810834
NM_000364.4(TNNT2):c.634C>T (p.Arg212Trp) rs45586240
NM_000364.4(TNNT2):c.63T>G (p.Val21=) rs397516477
NM_000364.4(TNNT2):c.68-5_68-3delinsTT rs397516362
NM_000364.4(TNNT2):c.68-8A>G rs115805892
NM_000364.4(TNNT2):c.68-9G>A rs1221903769
NM_000364.4(TNNT2):c.711-13C>G rs377714587
NM_000364.4(TNNT2):c.711-4G>T rs201753429
NM_000364.4(TNNT2):c.753G>T (p.Glu251Asp) rs45466197
NM_000364.4(TNNT2):c.779A>G (p.Lys260Arg) rs3730238
NM_000364.4(TNNT2):c.794A>T (p.Lys265Ile) rs397516482
NM_000364.4(TNNT2):c.801+5G>A rs730881113
NM_000364.4(TNNT2):c.806A>G (p.Asn269Ser) rs397516483
NM_000364.4(TNNT2):c.826A>G (p.Asn276Asp) rs4523540
NM_000364.4(TNNT2):c.828C>T (p.Asn276=) rs376923877
NM_000364.4(TNNT2):c.835dup (p.Gln279fs) rs730881119
NM_000364.4(TNNT2):c.853C>T (p.Arg285Cys) rs121964857
NM_000364.4(TNNT2):c.854G>C (p.Arg285Pro) rs397516484
NM_000364.4(TNNT2):c.855C>T (p.Arg285=) rs45503195
NM_000364.4(TNNT2):c.873C>T (p.Thr291=) rs45465693
NM_000364.4(TNNT2):c.90C>T (p.Asp30=) rs727503515
NM_000364.4(TNNT2):c.98-4C>G rs775895925

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