ClinVar Miner

List of variants in gene TNNI3 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 104
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HGVS dbSNP
NM_000363.5(TNNI3):c.107A>C (p.Lys36Thr) rs886039441
NM_000363.5(TNNI3):c.108+2T>G rs1057520417
NM_000363.5(TNNI3):c.108+59A>G rs143098258
NM_000363.5(TNNI3):c.109-132A>G rs73617693
NM_000363.5(TNNI3):c.109-17C>A rs139150276
NM_000363.5(TNNI3):c.109-20G>C rs1555864156
NM_000363.5(TNNI3):c.114A>T (p.Lys38Asn) rs730881066
NM_000363.5(TNNI3):c.114dup (p.Ser39fs) rs772607683
NM_000363.5(TNNI3):c.12-50_12-47dup rs377373012
NM_000363.5(TNNI3):c.12-7del rs370714315
NM_000363.5(TNNI3):c.131C>G (p.Ser44Trp) rs730881085
NM_000363.5(TNNI3):c.132G>C (p.Ser44=) rs727504941
NM_000363.5(TNNI3):c.139T>C (p.Leu47=) rs587780967
NM_000363.5(TNNI3):c.150G>A (p.Lys50=) rs730881086
NM_000363.5(TNNI3):c.151-6C>G rs377258542
NM_000363.5(TNNI3):c.19G>C (p.Asp7His) rs1201960520
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.208G>A (p.Gly70Arg) rs730881067
NM_000363.5(TNNI3):c.225T>G (p.Ala75=) rs1555864028
NM_000363.5(TNNI3):c.235C>T (p.Arg79Cys) rs3729712
NM_000363.5(TNNI3):c.24+19G>A rs368708903
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser) rs77615401
NM_000363.5(TNNI3):c.246G>T (p.Pro82=) rs397516343
NM_000363.5(TNNI3):c.25-4C>T rs202086705
NM_000363.5(TNNI3):c.264G>A (p.Leu88=) rs772928416
NM_000363.5(TNNI3):c.282+16_282+17delinsTT rs1555864004
NM_000363.5(TNNI3):c.282+6G>C rs1210217999
NM_000363.5(TNNI3):c.283-202G>T rs1005638211
NM_000363.5(TNNI3):c.283-221C>G rs140633085
NM_000363.5(TNNI3):c.292C>T (p.Arg98Ter) rs730881068
NM_000363.5(TNNI3):c.293G>A (p.Arg98Gln) rs747522089
NM_000363.5(TNNI3):c.302A>G (p.His101Arg) rs730881087
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872
NM_000363.5(TNNI3):c.308G>A (p.Arg103His) rs371000425
NM_000363.5(TNNI3):c.309T>C (p.Arg103=) rs749136271
NM_000363.5(TNNI3):c.331A>G (p.Arg111Gly) rs730881088
NM_000363.5(TNNI3):c.336C>T (p.Tyr112=) rs559450042
NM_000363.5(TNNI3):c.340A>G (p.Ile114Val) rs730881070
NM_000363.5(TNNI3):c.356C>T (p.Thr119Ile) rs184709702
NM_000363.5(TNNI3):c.363C>T (p.Asn121=) rs371490136
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506
NM_000363.5(TNNI3):c.372+20C>T rs529338677
NM_000363.5(TNNI3):c.373-15C>T rs192630178
NM_000363.5(TNNI3):c.373-16C>T rs373508654
NM_000363.5(TNNI3):c.384G>A (p.Leu128=) rs373130533
NM_000363.5(TNNI3):c.406C>T (p.Arg136Ter) rs1393946566
NM_000363.5(TNNI3):c.407G>A (p.Arg136Gln) rs730881069
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp) rs730881071
NM_000363.5(TNNI3):c.422G>A (p.Arg141Gln) rs397516347
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn) rs397516348
NM_000363.5(TNNI3):c.432G>T (p.Leu144=) rs776615304
NM_000363.5(TNNI3):c.433C>G (p.Arg145Gly) rs104894724
NM_000363.5(TNNI3):c.433C>T (p.Arg145Trp) rs104894724
NM_000363.5(TNNI3):c.434G>A (p.Arg145Gln) rs397516349
NM_000363.5(TNNI3):c.451G>A (p.Ala151Thr) rs730881072
NM_000363.5(TNNI3):c.458C>A (p.Ala153Asp) rs730881073
NM_000363.5(TNNI3):c.463A>G (p.Met155Val) rs730881074
NM_000363.5(TNNI3):c.470C>T (p.Ala157Val) rs397516353
NM_000363.5(TNNI3):c.471G>A (p.Ala157=) rs747756509
NM_000363.5(TNNI3):c.474G>C (p.Leu158=) rs749880457
NM_000363.5(TNNI3):c.484C>T (p.Arg162Trp) rs368861241
NM_000363.5(TNNI3):c.485G>A (p.Arg162Gln) rs397516354
NM_000363.5(TNNI3):c.493G>T (p.Glu165Ter) rs1057521530
NM_000363.5(TNNI3):c.497C>T (p.Ser166Phe) rs727504242
NM_000363.5(TNNI3):c.502G>A (p.Asp168Asn) rs1085308019
NM_000363.5(TNNI3):c.508C>T (p.Arg170Trp) rs727503504
NM_000363.5(TNNI3):c.509G>A (p.Arg170Gln) rs727503503
NM_000363.5(TNNI3):c.514C>G (p.His172Asp) rs730881075
NM_000363.5(TNNI3):c.521A>C (p.Lys174Thr) rs730881076
NM_000363.5(TNNI3):c.544G>A (p.Glu182Lys) rs397516355
NM_000363.5(TNNI3):c.547A>G (p.Lys183Glu) rs730881077
NM_000363.5(TNNI3):c.548A>C (p.Lys183Thr) rs730881078
NM_000363.5(TNNI3):c.549+128A>C rs10414696
NM_000363.5(TNNI3):c.549+211A>G rs10414493
NM_000363.5(TNNI3):c.549+267T>A rs11671448
NM_000363.5(TNNI3):c.550-157T>A rs114949974
NM_000363.5(TNNI3):c.550-256_550-255del rs56007758
NM_000363.5(TNNI3):c.553A>T (p.Asn185Tyr) rs730881089
NM_000363.5(TNNI3):c.554A>G (p.Asn185Ser) rs730881079
NM_000363.5(TNNI3):c.556C>T (p.Arg186Trp) rs760978512
NM_000363.5(TNNI3):c.557G>A (p.Arg186Gln) rs397516357
NM_000363.5(TNNI3):c.562G>A (p.Val188Met) rs193922409
NM_000363.5(TNNI3):c.562G>T (p.Val188Leu) rs193922409
NM_000363.5(TNNI3):c.570C>G (p.Asp190Glu) rs1131691856
NM_000363.5(TNNI3):c.575G>A (p.Arg192His) rs104894729
NM_000363.5(TNNI3):c.577A>G (p.Lys193Glu) rs730881080
NM_000363.5(TNNI3):c.579G>T (p.Lys193Asn) rs397516358
NM_000363.5(TNNI3):c.581A>G (p.Asn194Ser) rs730881081
NM_000363.5(TNNI3):c.582C>G (p.Asn194Lys) rs730881090
NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn) rs104894727
NM_000363.5(TNNI3):c.592C>G (p.Leu198Val) rs727504285
NM_000363.5(TNNI3):c.594G>C (p.Leu198=) rs1599907577
NM_000363.5(TNNI3):c.596G>A (p.Ser199Asn) rs730881091
NM_000363.5(TNNI3):c.609C>T (p.Gly203=) rs587780968
NM_000363.5(TNNI3):c.610C>T (p.Arg204Cys) rs727504243
NM_000363.5(TNNI3):c.611G>A (p.Arg204His) rs727504275
NM_000363.5(TNNI3):c.616A>G (p.Lys206Glu) rs104894725
NM_000363.5(TNNI3):c.617A>T (p.Lys206Ile) rs730881082
NM_000363.5(TNNI3):c.618A>G (p.Lys206=) rs1374789557
NM_000363.5(TNNI3):c.625G>A (p.Glu209Lys) rs727504268
NM_000363.5(TNNI3):c.626A>C (p.Glu209Ala) rs730881083
NM_000363.5(TNNI3):c.632G>T (p.Ter211Leu) rs730881084
NM_000363.5(TNNI3):c.6G>A (p.Ala2=) rs397516361
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr) rs796104366

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