ClinVar Miner

List of variants in gene TNNI3 reported as uncertain significance for Hypertrophic cardiomyopathy

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Total variants: 135
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HGVS dbSNP
NC_000019.10:g.(?_55151814)_(55154850_?)del
NC_000019.10:g.(?_55151824)_(55154840_?)del
NC_000019.10:g.(?_55151824)_(55157641_?)dup
NC_000019.10:g.(?_55154020)_(55156654_?)del
NM_000363.5(TNNI3):c.-103C>T rs557391836
NM_000363.5(TNNI3):c.-133G>T rs886054636
NM_000363.5(TNNI3):c.-85A>C rs186540595
NM_000363.5(TNNI3):c.104C>T (p.Ala35Val) rs1190447904
NM_000363.5(TNNI3):c.108+4G>T rs878853954
NM_000363.5(TNNI3):c.108+5G>A
NM_000363.5(TNNI3):c.108G>A (p.Lys36=)
NM_000363.5(TNNI3):c.109-7C>G rs1317507392
NM_000363.5(TNNI3):c.11+1G>T
NM_000363.5(TNNI3):c.114del (p.Lys38fs)
NM_000363.5(TNNI3):c.11G>A (p.Gly4Glu)
NM_000363.5(TNNI3):c.12-1G>A
NM_000363.5(TNNI3):c.12-7del rs370714315
NM_000363.5(TNNI3):c.125C>T (p.Ser42Phe)
NM_000363.5(TNNI3):c.128C>G (p.Ala43Gly)
NM_000363.5(TNNI3):c.131C>G (p.Ser44Trp) rs730881085
NM_000363.5(TNNI3):c.137A>T (p.Lys46Ile)
NM_000363.5(TNNI3):c.13A>G (p.Ser5Gly)
NM_000363.5(TNNI3):c.143A>C (p.Gln48Pro) rs200720341
NM_000363.5(TNNI3):c.150+1G>C
NM_000363.5(TNNI3):c.150G>A (p.Lys50=) rs730881086
NM_000363.5(TNNI3):c.157C>T (p.Leu53=) rs763981651
NM_000363.5(TNNI3):c.15C>A (p.Ser5Arg)
NM_000363.5(TNNI3):c.164A>C (p.Gln55Pro) rs775512887
NM_000363.5(TNNI3):c.167T>C (p.Ile56Thr) rs545441942
NM_000363.5(TNNI3):c.173A>G (p.Lys58Arg) rs878853955
NM_000363.5(TNNI3):c.184G>A (p.Glu62Lys) rs1357844466
NM_000363.5(TNNI3):c.190G>T (p.Glu64Ter) rs1245885836
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.205C>A (p.Arg69Ser) rs1555864037
NM_000363.5(TNNI3):c.217G>C (p.Gly73Arg)
NM_000363.5(TNNI3):c.220C>A (p.Arg74Ser)
NM_000363.5(TNNI3):c.236G>T (p.Arg79Leu) rs397516342
NM_000363.5(TNNI3):c.24+2T>A rs777702465
NM_000363.5(TNNI3):c.24+5G>C
NM_000363.5(TNNI3):c.24+6A>G
NM_000363.5(TNNI3):c.245C>T (p.Pro82Leu)
NM_000363.5(TNNI3):c.25-6A>G
NM_000363.5(TNNI3):c.258del (p.Leu88fs) rs727503507
NM_000363.5(TNNI3):c.278T>C (p.Leu93Pro) rs776035548
NM_000363.5(TNNI3):c.282+2T>A
NM_000363.5(TNNI3):c.282+5C>G rs770260866
NM_000363.5(TNNI3):c.282+6G>C rs1210217999
NM_000363.5(TNNI3):c.292C>T (p.Arg98Ter) rs730881068
NM_000363.5(TNNI3):c.298C>T (p.Leu100Phe) rs773216333
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872
NM_000363.5(TNNI3):c.307C>G (p.Arg103Gly) rs397516344
NM_000363.5(TNNI3):c.308G>A (p.Arg103His) rs371000425
NM_000363.5(TNNI3):c.308G>T (p.Arg103Leu) rs371000425
NM_000363.5(TNNI3):c.318G>C (p.Lys106Asn)
NM_000363.5(TNNI3):c.322G>A (p.Asp108Asn)
NM_000363.5(TNNI3):c.323A>T (p.Asp108Val) rs1555863719
NM_000363.5(TNNI3):c.331A>G (p.Arg111Gly) rs730881088
NM_000363.5(TNNI3):c.332G>T (p.Arg111Ile) rs1599909659
NM_000363.5(TNNI3):c.332_333del (p.Arg111fs) rs1555863715
NM_000363.5(TNNI3):c.340A>G (p.Ile114Val) rs730881070
NM_000363.5(TNNI3):c.347C>G (p.Ala116Gly) rs777177571
NM_000363.5(TNNI3):c.347C>T (p.Ala116Val)
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702
NM_000363.5(TNNI3):c.356C>T (p.Thr119Ile) 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.372+1G>A
NM_000363.5(TNNI3):c.373-11T>A
NM_000363.5(TNNI3):c.373A>T (p.Ile125Phe) rs1599909309
NM_000363.5(TNNI3):c.374T>C (p.Ile125Thr) rs878853956
NM_000363.5(TNNI3):c.389AGA[1] (p.Lys131del) rs1315063739
NM_000363.5(TNNI3):c.391A>G (p.Lys131Glu) rs1599909289
NM_000363.5(TNNI3):c.403C>T (p.Leu135Phe) rs1555863549
NM_000363.5(TNNI3):c.406C>T (p.Arg136Ter) rs1393946566
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp) rs730881071
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn) rs397516348
NM_000363.5(TNNI3):c.432_437dup (p.Arg145_Arg146dup)
NM_000363.5(TNNI3):c.434G>T (p.Arg145Leu)
NM_000363.5(TNNI3):c.440T>C (p.Val147Ala)
NM_000363.5(TNNI3):c.451G>A (p.Ala151Thr) rs730881072
NM_000363.5(TNNI3):c.479G>A (p.Gly160Glu)
NM_000363.5(TNNI3):c.481del (p.Ala161fs)
NM_000363.5(TNNI3):c.482C>T (p.Ala161Val) rs753413305
NM_000363.5(TNNI3):c.484C>A (p.Arg162=)
NM_000363.5(TNNI3):c.485_514del (p.Arg162_Ala171del) rs1555863489
NM_000363.5(TNNI3):c.487del (p.Ala163fs) rs1599909151
NM_000363.5(TNNI3):c.488C>T (p.Ala163Val) rs727504367
NM_000363.5(TNNI3):c.493G>C (p.Glu165Gln) rs1057521530
NM_000363.5(TNNI3):c.493G>T (p.Glu165Ter) rs1057521530
NM_000363.5(TNNI3):c.502G>C (p.Asp168His) rs1085308019
NM_000363.5(TNNI3):c.511G>A (p.Ala171Thr) rs121917761
NM_000363.5(TNNI3):c.512C>T (p.Ala171Val) rs1555863491
NM_000363.5(TNNI3):c.514C>T (p.His172Tyr) rs730881075
NM_000363.5(TNNI3):c.520A>C (p.Lys174Gln) rs1555863480
NM_000363.5(TNNI3):c.526G>A (p.Val176Met) rs727503501
NM_000363.5(TNNI3):c.533A>G (p.Lys178Arg)
NM_000363.5(TNNI3):c.536_549+1del
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.549+4A>T rs1197428009
NM_000363.5(TNNI3):c.550-1G>A rs1555863017
NM_000363.5(TNNI3):c.550-8T>A rs766762049
NM_000363.5(TNNI3):c.550G>C (p.Glu184Gln)
NM_000363.5(TNNI3):c.559_560delinsAG (p.Glu187Arg)
NM_000363.5(TNNI3):c.55A>G (p.Ile19Val) rs755862334
NM_000363.5(TNNI3):c.561G>T (p.Glu187Asp) rs773184959
NM_000363.5(TNNI3):c.563_569del (p.Val188fs)
NM_000363.5(TNNI3):c.577A>G (p.Lys193Glu) rs730881080
NM_000363.5(TNNI3):c.579G>C (p.Lys193Asn) rs397516358
NM_000363.5(TNNI3):c.581A>C (p.Asn194Thr) rs730881081
NM_000363.5(TNNI3):c.585C>G (p.Ile195Met)
NM_000363.5(TNNI3):c.587A>G (p.Asp196Gly)
NM_000363.5(TNNI3):c.595A>T (p.Ser199Cys)
NM_000363.5(TNNI3):c.599G>A (p.Gly200Glu) rs878853957
NM_000363.5(TNNI3):c.599G>T (p.Gly200Val) rs878853957
NM_000363.5(TNNI3):c.610C>A (p.Arg204Ser) rs727504243
NM_000363.5(TNNI3):c.61C>A (p.Arg21Ser) rs267607128
NM_000363.5(TNNI3):c.620A>G (p.Lys207Arg)
NM_000363.5(TNNI3):c.621G>C (p.Lys207Asn)
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.65G>A (p.Arg22His) rs397516360
NM_000363.5(TNNI3):c.65G>T (p.Arg22Leu) rs397516360
NM_000363.5(TNNI3):c.67T>C (p.Ser23Pro) rs1555864374
NM_000363.5(TNNI3):c.70T>A (p.Ser24Thr)
NM_000363.5(TNNI3):c.74A>C (p.Asn25Thr) rs1555864368
NM_000363.5(TNNI3):c.79C>G (p.Arg27Gly) rs1555864366
NM_000363.5(TNNI3):c.79C>T (p.Arg27Cys)
NM_000363.5(TNNI3):c.7G>T (p.Asp3Tyr)
NM_000363.5(TNNI3):c.86A>G (p.Tyr29Cys)
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr) rs796104366
NM_000363.5(TNNI3):c.92C>T (p.Thr31Met) rs201928445
NM_000363.5(TNNI3):c.98C>A (p.Pro33Gln)
NM_000363.5(TNNI3):c.99_100dup (p.His34fs)
Single allele

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