ClinVar Miner

List of variants in gene TNNI3 reported as likely benign for Cardiomyopathy

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Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser) rs77615401 0.00699
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.363C>T (p.Asn121=) rs371490136 0.00006
NM_000363.5(TNNI3):c.39C>G (p.Arg13=) rs397516346 0.00005
NM_000363.5(TNNI3):c.303C>T (p.His101=) rs199539066 0.00004
NM_000363.5(TNNI3):c.6G>A (p.Ala2=) rs397516361 0.00004
NM_000363.5(TNNI3):c.-8G>A rs773513015 0.00003
NM_000363.5(TNNI3):c.373-13C>T rs771031464 0.00003
NM_000363.5(TNNI3):c.516C>T (p.His172=) rs764527627 0.00003
NM_000363.5(TNNI3):c.93G>C (p.Thr31=) rs765719980 0.00003
NM_000363.5(TNNI3):c.151-6C>G rs377258542 0.00002
NM_000363.5(TNNI3):c.202C>A (p.Arg68=) rs772695512 0.00002
NM_000363.5(TNNI3):c.283-9C>T rs759922995 0.00002
NM_000363.5(TNNI3):c.471G>A (p.Ala157=) rs747756509 0.00002
NM_000363.5(TNNI3):c.226C>T (p.Leu76=) rs1336868426 0.00001
NM_000363.5(TNNI3):c.24+6A>G rs1178267975 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.336C>T (p.Tyr112=) rs559450042 0.00001
NM_000363.5(TNNI3):c.340A>G (p.Ile114Val) rs730881070 0.00001
NM_000363.5(TNNI3):c.384G>A (p.Leu128=) rs373130533 0.00001
NM_000363.5(TNNI3):c.432G>C (p.Leu144=) rs776615304 0.00001
NM_000363.5(TNNI3):c.474G>C (p.Leu158=) rs749880457 0.00001
NM_000363.5(TNNI3):c.550-12G>A rs754944128 0.00001
NM_000363.5(TNNI3):c.550-13C>T rs372398075 0.00001
NM_000363.5(TNNI3):c.550-14T>C rs758992431 0.00001
NM_000363.5(TNNI3):c.55A>G (p.Ile19Val) rs755862334 0.00001
NM_000363.5(TNNI3):c.585C>T (p.Ile195=) rs200085986 0.00001
NM_000363.5(TNNI3):c.606G>A (p.Glu202=) rs796474405 0.00001
NM_000363.5(TNNI3):c.*3C>T rs1568856984
NM_000363.5(TNNI3):c.109-15A>G rs779144176
NM_000363.5(TNNI3):c.12-4C>T rs769896482
NM_000363.5(TNNI3):c.120G>A (p.Lys40=) rs2085732703
NM_000363.5(TNNI3):c.129C>T (p.Ala43=)
NM_000363.5(TNNI3):c.12G>A (p.Gly4=)
NM_000363.5(TNNI3):c.151-12A>C rs2085729835
NM_000363.5(TNNI3):c.156G>A (p.Leu52=) rs2085729640
NM_000363.5(TNNI3):c.157C>T (p.Leu53=) rs763981651
NM_000363.5(TNNI3):c.201G>A (p.Glu67=)
NM_000363.5(TNNI3):c.207C>A (p.Arg69=)
NM_000363.5(TNNI3):c.234C>A (p.Thr78=)
NM_000363.5(TNNI3):c.279G>A (p.Leu93=) rs1568859087
NM_000363.5(TNNI3):c.283-13G>T rs552152124
NM_000363.5(TNNI3):c.28A>G (p.Arg10Gly) rs2085739021
NM_000363.5(TNNI3):c.294A>G (p.Arg98=) rs1568858567
NM_000363.5(TNNI3):c.318G>A (p.Lys106=) rs750350912
NM_000363.5(TNNI3):c.330G>A (p.Glu110=) rs1010374485
NM_000363.5(TNNI3):c.345G>A (p.Glu115=) rs1568858500
NM_000363.5(TNNI3):c.354C>T (p.Val118=) rs2085716325
NM_000363.5(TNNI3):c.357C>G (p.Thr119=)
NM_000363.5(TNNI3):c.373-12G>A
NM_000363.5(TNNI3):c.373-14del rs1472113441
NM_000363.5(TNNI3):c.373-8G>A rs369244036
NM_000363.5(TNNI3):c.402C>T (p.Asp134=) rs2085712789
NM_000363.5(TNNI3):c.432G>T (p.Leu144=) rs776615304
NM_000363.5(TNNI3):c.441G>C (p.Val147=) rs2085712211
NM_000363.5(TNNI3):c.508C>A (p.Arg170=) rs727503504
NM_000363.5(TNNI3):c.522G>A (p.Lys174=) rs730880231
NM_000363.5(TNNI3):c.567A>G (p.Gly189=) rs902161211
NM_000363.5(TNNI3):c.612C>G (p.Arg204=) rs1599907540
NM_000363.5(TNNI3):c.9T>C (p.Asp3=) rs2085744143

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