ClinVar Miner

List of variants in gene TNNI3 reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 37
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HGVS dbSNP
NM_000363.5(TNNI3):c.109-15A>G rs779144176
NM_000363.5(TNNI3):c.127G>T (p.Ala43Ser) rs727505023
NM_000363.5(TNNI3):c.151-6C>G rs377258542
NM_000363.5(TNNI3):c.167T>C (p.Ile56Thr) rs545441942
NM_000363.5(TNNI3):c.168T>G (p.Ile56Met) rs727503509
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.233C>T (p.Thr78Ile) rs786205288
NM_000363.5(TNNI3):c.236G>T (p.Arg79Leu) rs397516342
NM_000363.5(TNNI3):c.258del (p.Leu88fs) rs727503507
NM_000363.5(TNNI3):c.307C>T (p.Arg103Cys) rs397516344
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702
NM_000363.5(TNNI3):c.368C>T (p.Thr123Met) rs397516345
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506
NM_000363.5(TNNI3):c.401A>G (p.Asp134Gly) rs727503505
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn) rs397516348
NM_000363.5(TNNI3):c.462G>A (p.Met154Ile) rs397516350
NM_000363.5(TNNI3):c.488C>T (p.Ala163Val) rs727504367
NM_000363.5(TNNI3):c.508C>G (p.Arg170Gly) rs727503504
NM_000363.5(TNNI3):c.525G>C (p.Gln175His) rs727503502
NM_000363.5(TNNI3):c.526G>A (p.Val176Met) rs727503501
NM_000363.5(TNNI3):c.538del (p.Asp180fs) rs876658023
NM_000363.5(TNNI3):c.539A>G (p.Asp180Gly) rs1060499912
NM_000363.5(TNNI3):c.559G>A (p.Glu187Lys) rs727505069
NM_000363.5(TNNI3):c.579G>C (p.Lys193Asn) rs397516358
NM_000363.5(TNNI3):c.583A>C (p.Ile195Leu) rs876658024
NM_000363.5(TNNI3):c.586G>T (p.Asp196Tyr) rs104894727
NM_000363.5(TNNI3):c.592C>G (p.Leu198Val) rs727504285
NM_000363.5(TNNI3):c.5C>T (p.Ala2Val) rs397516359
NM_000363.5(TNNI3):c.610C>T (p.Arg204Cys) rs727504243
NM_000363.5(TNNI3):c.613A>C (p.Lys205Gln) rs727505331
NM_000363.5(TNNI3):c.622T>A (p.Phe208Ile) rs876658025
NM_000363.5(TNNI3):c.624T>G (p.Phe208Leu) rs876658026
NM_000363.5(TNNI3):c.625G>A (p.Glu209Lys) rs727504268
NM_000363.5(TNNI3):c.632G>T (p.Ter211Leu) rs730881084
NM_000363.5(TNNI3):c.65G>A (p.Arg22His) rs397516360
NM_000363.5(TNNI3):c.79C>G (p.Arg27Gly) rs1555864366
NM_000363.5(TNNI3):c.85T>G (p.Tyr29Asp) rs727503510

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