ClinVar Miner

List of variants in gene TNNI3 reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 131
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HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.198G>A (p.Glu66=) rs3729710 0.03372
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser) rs77615401 0.00699
NM_000363.5(TNNI3):c.273G>A (p.Ala91=) rs75491697 0.00198
NM_000363.5(TNNI3):c.25-4C>T rs202086705 0.00069
NM_000363.5(TNNI3):c.235C>T (p.Arg79Cys) rs3729712 0.00048
NM_000363.5(TNNI3):c.132G>C (p.Ser44=) rs727504941 0.00012
NM_000363.5(TNNI3):c.207C>G (p.Arg69=) rs201422579 0.00012
NM_000363.5(TNNI3):c.246G>T (p.Pro82=) rs397516343 0.00007
NM_000363.5(TNNI3):c.373-4C>G rs2288530 0.00007
NM_000363.5(TNNI3):c.139T>C (p.Leu47=) rs587780967 0.00006
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702 0.00006
NM_000363.5(TNNI3):c.363C>T (p.Asn121=) rs371490136 0.00006
NM_000363.5(TNNI3):c.39C>G (p.Arg13=) rs397516346 0.00005
NM_000363.5(TNNI3):c.282+5C>G rs770260866 0.00004
NM_000363.5(TNNI3):c.292C>T (p.Arg98Ter) rs730881068 0.00004
NM_000363.5(TNNI3):c.293G>A (p.Arg98Gln) rs747522089 0.00004
NM_000363.5(TNNI3):c.303C>T (p.His101=) rs199539066 0.00004
NM_000363.5(TNNI3):c.308G>A (p.Arg103His) rs371000425 0.00004
NM_000363.5(TNNI3):c.422G>A (p.Arg141Gln) rs397516347 0.00004
NM_000363.5(TNNI3):c.484C>T (p.Arg162Trp) rs368861241 0.00004
NM_000363.5(TNNI3):c.6G>A (p.Ala2=) rs397516361 0.00004
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872 0.00003
NM_000363.5(TNNI3):c.93G>C (p.Thr31=) rs765719980 0.00003
NM_000363.5(TNNI3):c.143A>C (p.Gln48Pro) rs200720341 0.00002
NM_000363.5(TNNI3):c.434G>A (p.Arg145Gln) rs397516349 0.00002
NM_000363.5(TNNI3):c.471G>A (p.Ala157=) rs747756509 0.00002
NM_000363.5(TNNI3):c.92C>T (p.Thr31Met) rs201928445 0.00002
NM_000363.5(TNNI3):c.146dup (p.Lys50fs) rs1162696593 0.00001
NM_000363.5(TNNI3):c.167T>C (p.Ile56Thr) rs545441942 0.00001
NM_000363.5(TNNI3):c.213G>A (p.Glu71=) rs770487905 0.00001
NM_000363.5(TNNI3):c.250G>T (p.Glu84Ter) rs759523214 0.00001
NM_000363.5(TNNI3):c.277C>T (p.Leu93=) rs1221536494 0.00001
NM_000363.5(TNNI3):c.300C>G (p.Leu100=) rs772145171 0.00001
NM_000363.5(TNNI3):c.307C>T (p.Arg103Cys) rs397516344 0.00001
NM_000363.5(TNNI3):c.322G>A (p.Asp108Asn) rs766958196 0.00001
NM_000363.5(TNNI3):c.331A>G (p.Arg111Gly) rs730881088 0.00001
NM_000363.5(TNNI3):c.340A>G (p.Ile114Val) rs730881070 0.00001
NM_000363.5(TNNI3):c.341T>C (p.Ile114Thr) rs762692450 0.00001
NM_000363.5(TNNI3):c.34C>T (p.Pro12Ser) rs553214254 0.00001
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506 0.00001
NM_000363.5(TNNI3):c.417T>C (p.Phe139=) rs1371643118 0.00001
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp) rs730881071 0.00001
NM_000363.5(TNNI3):c.426C>T (p.Pro142=) rs532949659 0.00001
NM_000363.5(TNNI3):c.474G>C (p.Leu158=) rs749880457 0.00001
NM_000363.5(TNNI3):c.482C>T (p.Ala161Val) rs753413305 0.00001
NM_000363.5(TNNI3):c.485G>A (p.Arg162Gln) rs397516354 0.00001
NM_000363.5(TNNI3):c.497C>T (p.Ser166Phe) rs727504242 0.00001
NM_000363.5(TNNI3):c.557G>A (p.Arg186Gln) rs397516357 0.00001
NM_000363.5(TNNI3):c.585C>T (p.Ile195=) rs200085986 0.00001
NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn) rs104894727 0.00001
NM_000363.5(TNNI3):c.592C>G (p.Leu198Val) rs727504285 0.00001
NM_000363.5(TNNI3):c.604G>C (p.Glu202Gln) rs1470970097 0.00001
NM_000363.5(TNNI3):c.108+5G>A rs1261858318
NM_000363.5(TNNI3):c.11+4A>G
NM_000363.5(TNNI3):c.114A>T (p.Lys38Asn) rs730881066
NM_000363.5(TNNI3):c.115T>C (p.Ser39Pro)
NM_000363.5(TNNI3):c.119A>T (p.Lys40Met)
NM_000363.5(TNNI3):c.11G>A (p.Gly4Glu) rs1351385449
NM_000363.5(TNNI3):c.130T>A (p.Ser44Thr)
NM_000363.5(TNNI3):c.131C>G (p.Ser44Trp) rs730881085
NM_000363.5(TNNI3):c.134G>A (p.Arg45Lys) rs2147285293
NM_000363.5(TNNI3):c.146T>A (p.Leu49Gln)
NM_000363.5(TNNI3):c.151A>G (p.Thr51Ala)
NM_000363.5(TNNI3):c.16A>G (p.Ser6Gly)
NM_000363.5(TNNI3):c.173A>G (p.Lys58Arg) rs878853955
NM_000363.5(TNNI3):c.190G>C (p.Glu64Gln)
NM_000363.5(TNNI3):c.194C>T (p.Ala65Val) rs1057518784
NM_000363.5(TNNI3):c.201G>A (p.Glu67=)
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.207C>T (p.Arg69=) rs201422579
NM_000363.5(TNNI3):c.220C>A (p.Arg74Ser) rs375795196
NM_000363.5(TNNI3):c.220C>G (p.Arg74Gly)
NM_000363.5(TNNI3):c.220C>T (p.Arg74Cys) rs375795196
NM_000363.5(TNNI3):c.221G>C (p.Arg74Pro) rs886039022
NM_000363.5(TNNI3):c.227T>C (p.Leu76Pro) rs1443859469
NM_000363.5(TNNI3):c.232A>T (p.Thr78Ser) rs786204399
NM_000363.5(TNNI3):c.258del (p.Leu88fs) rs727503507
NM_000363.5(TNNI3):c.269T>G (p.Phe90Cys)
NM_000363.5(TNNI3):c.318G>C (p.Lys106Asn) rs750350912
NM_000363.5(TNNI3):c.335dup (p.Tyr112Ter)
NM_000363.5(TNNI3):c.337G>A (p.Asp113Asn) rs779064799
NM_000363.5(TNNI3):c.339C>T (p.Asp113=) rs786204400
NM_000363.5(TNNI3):c.356C>T (p.Thr119Ile) rs184709702
NM_000363.5(TNNI3):c.372+2T>A
NM_000363.5(TNNI3):c.372+4G>C
NM_000363.5(TNNI3):c.380A>G (p.Asp127Gly)
NM_000363.5(TNNI3):c.382C>G (p.Leu128Val)
NM_000363.5(TNNI3):c.393G>A (p.Lys131=)
NM_000363.5(TNNI3):c.403C>T (p.Leu135Phe) rs1555863549
NM_000363.5(TNNI3):c.406C>G (p.Arg136Gly)
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.410G>A (p.Gly137Asp)
NM_000363.5(TNNI3):c.421C>G (p.Arg141Gly) rs730881071
NM_000363.5(TNNI3):c.433C>G (p.Arg145Gly) rs104894724
NM_000363.5(TNNI3):c.444G>A (p.Arg148=)
NM_000363.5(TNNI3):c.451G>A (p.Ala151Thr) rs730881072
NM_000363.5(TNNI3):c.470C>T (p.Ala157Val) rs397516353
NM_000363.5(TNNI3):c.485G>C (p.Arg162Pro) rs397516354
NM_000363.5(TNNI3):c.497C>G (p.Ser166Cys) rs727504242
NM_000363.5(TNNI3):c.502G>A (p.Asp168Asn) rs1085308019
NM_000363.5(TNNI3):c.509G>A (p.Arg170Gln) rs727503503
NM_000363.5(TNNI3):c.519C>T (p.Leu173=)
NM_000363.5(TNNI3):c.523C>T (p.Gln175Ter) rs876661394
NM_000363.5(TNNI3):c.525G>A (p.Gln175=)
NM_000363.5(TNNI3):c.534G>T (p.Lys178Asn)
NM_000363.5(TNNI3):c.538G>A (p.Asp180Asn) rs1060503103
NM_000363.5(TNNI3):c.539A>G (p.Asp180Gly) rs1060499912
NM_000363.5(TNNI3):c.547_548delinsGT (p.Lys183Val)
NM_000363.5(TNNI3):c.549+4_549+7del
NM_000363.5(TNNI3):c.55A>C (p.Ile19Leu) rs755862334
NM_000363.5(TNNI3):c.566G>C (p.Gly189Ala)
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.581A>C (p.Asn194Thr) rs730881081
NM_000363.5(TNNI3):c.595A>T (p.Ser199Cys) rs2085696801
NM_000363.5(TNNI3):c.596G>A (p.Ser199Asn) rs730881091
NM_000363.5(TNNI3):c.605A>G (p.Glu202Gly)
NM_000363.5(TNNI3):c.611G>A (p.Arg204His) rs727504275
NM_000363.5(TNNI3):c.614A>C (p.Lys205Thr) rs1555862962
NM_000363.5(TNNI3):c.61C>T (p.Arg21Cys) rs267607128
NM_000363.5(TNNI3):c.626A>C (p.Glu209Ala) rs730881083
NM_000363.5(TNNI3):c.629G>A (p.Ser210Asn)
NM_000363.5(TNNI3):c.63C>G (p.Arg21=) rs1555864377
NM_000363.5(TNNI3):c.79C>G (p.Arg27Gly) rs1555864366
NM_000363.5(TNNI3):c.79C>T (p.Arg27Cys) rs1555864366
NM_000363.5(TNNI3):c.80G>C (p.Arg27Pro) rs2147285955
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr) rs796104366
NM_000363.5(TNNI3):c.93G>A (p.Thr31=)
NM_000363.5(TNNI3):c.95A>G (p.Glu32Gly)
NM_000363.5(TNNI3):c.9T>A (p.Asp3Glu)

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