ClinVar Miner

List of variants in gene TNNI3 studied for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 189
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.12-129A>G rs11671293 0.36524
NM_000363.5(TNNI3):c.11+128T>C rs11667847 0.21853
NM_000363.5(TNNI3):c.11+99C>G rs3729708 0.09027
NM_000363.5(TNNI3):c.151-106A>G rs3729709 0.07534
NM_000363.5(TNNI3):c.109-132A>G rs73617693 0.07431
NM_000363.5(TNNI3):c.549+211A>G rs10414493 0.06837
NM_000363.5(TNNI3):c.109-185A>C rs2278281 0.06191
NM_000363.5(TNNI3):c.108+21G>A rs3729837 0.04872
NC_000019.10:g.55151563T>G rs73935312 0.03615
NM_000363.5(TNNI3):c.198G>A (p.Glu66=) rs3729710 0.03372
NM_000363.5(TNNI3):c.549+128A>C rs10414696 0.03166
NM_000363.5(TNNI3):c.108+182C>G rs28526132 0.02827
NM_000363.5(TNNI3):c.283-221C>G rs140633085 0.01308
NM_000363.5(TNNI3):c.108+59A>G rs143098258 0.01257
NM_000363.5(TNNI3):c.550-157T>A rs114949974 0.00877
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser) rs77615401 0.00699
NM_000363.4(TNNI3):c.-148A>G rs73935313 0.00695
NM_000363.5(TNNI3):c.-47C>T rs202159627 0.00625
NM_000363.5(TNNI3):c.109-170G>A rs189301935 0.00565
NC_000019.10:g.55151728G>T rs143032168 0.00555
NC_000019.10:g.55151712T>C rs142223367 0.00553
NM_000363.5(TNNI3):c.372+200C>G rs140862371 0.00386
NM_000363.5(TNNI3):c.373-43G>A rs183956525 0.00343
NM_000363.5(TNNI3):c.550-112T>C rs140242923 0.00338
NM_000363.5(TNNI3):c.283-202G>T rs1005638211 0.00236
NM_000363.5(TNNI3):c.273G>A (p.Ala91=) rs75491697 0.00198
NM_000363.5(TNNI3):c.550-10C>T rs201240150 0.00190
NM_000363.5(TNNI3):c.549+267T>A rs11671448 0.00175
NM_000363.5(TNNI3):c.109-17C>A rs139150276 0.00147
NM_000363.5(TNNI3):c.-85A>C rs186540595 0.00142
NM_000363.5(TNNI3):c.373-15C>G rs192630178 0.00141
NM_000363.5(TNNI3):c.-103C>T rs557391836 0.00102
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.373-16C>T rs373508654 0.00021
NM_000363.5(TNNI3):c.207C>G (p.Arg69=) rs201422579 0.00012
NM_000363.5(TNNI3):c.373-4C>G rs2288530 0.00007
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.276G>A (p.Glu92=) rs1407023193 0.00005
NM_000363.5(TNNI3):c.39C>G (p.Arg13=) rs397516346 0.00005
NM_000363.5(TNNI3):c.*35C>T rs375447438 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.556C>T (p.Arg186Trp) rs760978512 0.00004
NM_000363.5(TNNI3):c.-17C>A rs1439592517 0.00003
NM_000363.5(TNNI3):c.-8G>A rs773513015 0.00003
NM_000363.5(TNNI3):c.*16G>A rs778220410 0.00002
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.434G>A (p.Arg145Gln) rs397516349 0.00002
NM_000363.5(TNNI3):c.439G>C (p.Val147Leu) rs777782551 0.00002
NM_000363.5(TNNI3):c.543C>T (p.Thr181=) rs926550445 0.00002
NM_000363.5(TNNI3):c.92C>T (p.Thr31Met) rs201928445 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.167T>C (p.Ile56Thr) rs545441942 0.00001
NM_000363.5(TNNI3):c.217G>C (p.Gly73Arg) rs1170054667 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.341T>C (p.Ile114Thr) rs762692450 0.00001
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506 0.00001
NM_000363.5(TNNI3):c.372+20C>T rs529338677 0.00001
NM_000363.5(TNNI3):c.384G>A (p.Leu128=) rs373130533 0.00001
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp) rs730881071 0.00001
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn) rs397516348 0.00001
NM_000363.5(TNNI3):c.432G>C (p.Leu144=) rs776615304 0.00001
NM_000363.5(TNNI3):c.433C>T (p.Arg145Trp) rs104894724 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.485G>A (p.Arg162Gln) rs397516354 0.00001
NM_000363.5(TNNI3):c.493G>T (p.Glu165Ter) rs1057521530 0.00001
NM_000363.5(TNNI3):c.495G>A (p.Glu165=) rs1333619884 0.00001
NM_000363.5(TNNI3):c.497C>T (p.Ser166Phe) rs727504242 0.00001
NM_000363.5(TNNI3):c.550-14T>C rs758992431 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.606G>A (p.Glu202=) rs796474405 0.00001
NM_000363.5(TNNI3):c.610C>T (p.Arg204Cys) rs727504243 0.00001
NM_000363.5(TNNI3):c.632G>T (p.Ter211Leu) rs730881084 0.00001
NC_000019.10:g.55151632C>A rs2147281499
NM_000363.5(TNNI3):c.-60G>A rs2147286810
NM_000363.5(TNNI3):c.-98C>A rs12973773
NM_000363.5(TNNI3):c.107A>C (p.Lys36Thr) rs886039441
NM_000363.5(TNNI3):c.108+108G>C rs3729838
NM_000363.5(TNNI3):c.108+8G>T rs754020806
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.123C>G (p.Ile41Met) rs1311862702
NM_000363.5(TNNI3):c.127G>A (p.Ala43Thr) rs727505023
NM_000363.5(TNNI3):c.131C>G (p.Ser44Trp) rs730881085
NM_000363.5(TNNI3):c.173A>G (p.Lys58Arg) rs878853955
NM_000363.5(TNNI3):c.175C>T (p.Gln59Ter)
NM_000363.5(TNNI3):c.184G>A (p.Glu62Lys) rs1357844466
NM_000363.5(TNNI3):c.196GAG[1] (p.Glu67del)
NM_000363.5(TNNI3):c.19G>C (p.Asp7His) rs1201960520
NM_000363.5(TNNI3):c.1A>G (p.Met1Val) rs397516341
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.228G>A (p.Leu76=) rs1599911087
NM_000363.5(TNNI3):c.232A>T (p.Thr78Ser) rs786204399
NM_000363.5(TNNI3):c.233C>G (p.Thr78Ser) rs786205288
NM_000363.5(TNNI3):c.24+5G>C rs2085740818
NM_000363.5(TNNI3):c.258del (p.Leu88fs) rs727503507
NM_000363.5(TNNI3):c.294A>G (p.Arg98=) rs1568858567
NM_000363.5(TNNI3):c.302A>G (p.His101Arg) rs730881087
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.373-115G>C rs2288529
NM_000363.5(TNNI3):c.373-4C>T rs2288530
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.407G>A (p.Arg136Gln) rs730881069
NM_000363.5(TNNI3):c.422G>T (p.Arg141Leu) rs397516347
NM_000363.5(TNNI3):c.433C>G (p.Arg145Gly) rs104894724
NM_000363.5(TNNI3):c.451G>A (p.Ala151Thr) rs730881072
NM_000363.5(TNNI3):c.455A>G (p.Asp152Gly)
NM_000363.5(TNNI3):c.458C>A (p.Ala153Asp) rs730881073
NM_000363.5(TNNI3):c.470C>T (p.Ala157Val) rs397516353
NM_000363.5(TNNI3):c.488C>G (p.Ala163Gly) rs727504367
NM_000363.5(TNNI3):c.488C>T (p.Ala163Val) 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.502G>A (p.Asp168Asn) rs1085308019
NM_000363.5(TNNI3):c.506T>C (p.Leu169Pro) rs2147283204
NM_000363.5(TNNI3):c.508C>A (p.Arg170=) rs727503504
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.514C>T (p.His172Tyr) rs730881075
NM_000363.5(TNNI3):c.521A>C (p.Lys174Thr) rs730881076
NM_000363.5(TNNI3):c.522G>A (p.Lys174=) rs730880231
NM_000363.5(TNNI3):c.523C>T (p.Gln175Ter) rs876661394
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.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+68_549+69insGGCCTA rs139158921
NM_000363.5(TNNI3):c.550-106_550-105insAGAC rs542316818
NM_000363.5(TNNI3):c.550-256_550-255del rs56007758
NM_000363.5(TNNI3):c.550-2A>T
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.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.574C>T (p.Arg192Cys) rs727503499
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.583A>C (p.Ile195Leu) rs876658024
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.5C>T (p.Ala2Val) rs397516359
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.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.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.87T>A (p.Tyr29Ter)
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr) rs796104366
NM_000363.5(TNNI3):c.97C>A (p.Pro33Thr) rs1379608043

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.