ClinVar Miner

List of variants in gene TNNI3 reported as uncertain significance for Cardiovascular phenotype

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702 0.00006
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.308G>A (p.Arg103His) rs371000425 0.00004
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872 0.00003
NM_000363.5(TNNI3):c.143A>C (p.Gln48Pro) rs200720341 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.250G>T (p.Glu84Ter) rs759523214 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.341T>C (p.Ile114Thr) rs762692450 0.00001
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506 0.00001
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp) rs730881071 0.00001
NM_000363.5(TNNI3):c.482C>T (p.Ala161Val) rs753413305 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.130T>A (p.Ser44Thr)
NM_000363.5(TNNI3):c.131C>G (p.Ser44Trp) rs730881085
NM_000363.5(TNNI3):c.146T>A (p.Leu49Gln)
NM_000363.5(TNNI3):c.151A>G (p.Thr51Ala)
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.204del (p.Arg69fs) rs727504872
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.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.410G>A (p.Gly137Asp)
NM_000363.5(TNNI3):c.421C>G (p.Arg141Gly) rs730881071
NM_000363.5(TNNI3):c.451G>A (p.Ala151Thr) rs730881072
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.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.577A>G (p.Lys193Glu) rs730881080
NM_000363.5(TNNI3):c.581A>C (p.Asn194Thr) rs730881081
NM_000363.5(TNNI3):c.605A>G (p.Glu202Gly)
NM_000363.5(TNNI3):c.614A>C (p.Lys205Thr) rs1555862962
NM_000363.5(TNNI3):c.626A>C (p.Glu209Ala) rs730881083
NM_000363.5(TNNI3):c.629G>A (p.Ser210Asn)
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.95A>G (p.Glu32Gly)
NM_000363.5(TNNI3):c.9T>A (p.Asp3Glu)

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.