ClinVar Miner

List of variants in gene TNNI3 reported as uncertain significance for not provided

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Gene type:
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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702 0.00006
NM_000363.5(TNNI3):c.276G>A (p.Glu92=) rs1407023193 0.00005
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.308G>A (p.Arg103His) rs371000425 0.00004
NM_000363.5(TNNI3):c.143A>C (p.Gln48Pro) rs200720341 0.00002
NM_000363.5(TNNI3):c.151-6C>G rs377258542 0.00002
NM_000363.5(TNNI3):c.108+2T>G rs1057520417 0.00001
NM_000363.5(TNNI3):c.11+1G>T rs2085744080 0.00001
NM_000363.5(TNNI3):c.150G>A (p.Lys50=) rs730881086 0.00001
NM_000363.5(TNNI3):c.307C>T (p.Arg103Cys) rs397516344 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.370G>C (p.Glu124Gln) rs727503506 0.00001
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn) rs397516348 0.00001
NM_000363.5(TNNI3):c.463A>G (p.Met155Val) rs730881074 0.00001
NM_000363.5(TNNI3):c.482C>T (p.Ala161Val) rs753413305 0.00001
NM_000363.5(TNNI3):c.493G>T (p.Glu165Ter) rs1057521530 0.00001
NM_000363.5(TNNI3):c.604G>C (p.Glu202Gln) rs1470970097 0.00001
NM_000363.5(TNNI3):c.632G>T (p.Ter211Leu) rs730881084 0.00001
NM_000363.5(TNNI3):c.107A>C (p.Lys36Thr) rs886039441
NM_000363.5(TNNI3):c.114dup (p.Ser39fs) rs772607683
NM_000363.5(TNNI3):c.123C>G (p.Ile41Met) rs1311862702
NM_000363.5(TNNI3):c.175C>T (p.Gln59Ter)
NM_000363.5(TNNI3):c.184G>A (p.Glu62Lys) rs1357844466
NM_000363.5(TNNI3):c.19G>C (p.Asp7His) rs1201960520
NM_000363.5(TNNI3):c.200A>T (p.Glu67Val)
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.208G>A (p.Gly70Arg) rs730881067
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.224C>T (p.Ala75Val) rs1599911098
NM_000363.5(TNNI3):c.233C>G (p.Thr78Ser) rs786205288
NM_000363.5(TNNI3):c.294A>G (p.Arg98=) rs1568858567
NM_000363.5(TNNI3):c.328_329delinsAC (p.Glu110Thr) rs2147283705
NM_000363.5(TNNI3):c.356C>T (p.Thr119Ile) rs184709702
NM_000363.5(TNNI3):c.370G>A (p.Glu124Lys) rs727503506
NM_000363.5(TNNI3):c.386C>T (p.Thr129Ile) rs2147283314
NM_000363.5(TNNI3):c.389AGA[1] (p.Lys131del) rs1315063739
NM_000363.5(TNNI3):c.38G>A (p.Arg13His) rs2085738889
NM_000363.5(TNNI3):c.406C>T (p.Arg136Ter) rs1393946566
NM_000363.5(TNNI3):c.422G>T (p.Arg141Leu) rs397516347
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.488C>G (p.Ala163Gly) rs727504367
NM_000363.5(TNNI3):c.490A>G (p.Lys164Glu)
NM_000363.5(TNNI3):c.500T>C (p.Leu167Pro) rs1391407750
NM_000363.5(TNNI3):c.506T>C (p.Leu169Pro) rs2147283204
NM_000363.5(TNNI3):c.514C>T (p.His172Tyr) rs730881075
NM_000363.5(TNNI3):c.529AAG[1] (p.Lys178del) rs397516351
NM_000363.5(TNNI3):c.533A>G (p.Lys178Arg) rs2085711157
NM_000363.5(TNNI3):c.539A>G (p.Asp180Gly) rs1060499912
NM_000363.5(TNNI3):c.553A>T (p.Asn185Tyr) rs730881089
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.577A>G (p.Lys193Glu) rs730881080
NM_000363.5(TNNI3):c.583A>C (p.Ile195Leu) rs876658024
NM_000363.5(TNNI3):c.5C>T (p.Ala2Val) rs397516359
NM_000363.5(TNNI3):c.614A>C (p.Lys205Thr) rs1555862962
NM_000363.5(TNNI3):c.624dup (p.Glu209Ter) rs1599907512
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.67T>C (p.Ser23Pro) rs1555864374
NM_000363.5(TNNI3):c.74A>G (p.Asn25Ser)
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr) rs796104366
NM_000363.5(TNNI3):c.97C>A (p.Pro33Thr) rs1379608043

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