ClinVar Miner

List of variants in gene TNNI3 reported as likely benign by Color Health, Inc

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP
NM_000363.5(TNNI3):c.*3C>T rs1568856984
NM_000363.5(TNNI3):c.-8G>A
NM_000363.5(TNNI3):c.109-15A>G rs779144176
NM_000363.5(TNNI3):c.12-4C>T
NM_000363.5(TNNI3):c.120G>A (p.Lys40=)
NM_000363.5(TNNI3):c.132G>C (p.Ser44=) rs727504941
NM_000363.5(TNNI3):c.139T>C (p.Leu47=) rs587780967
NM_000363.5(TNNI3):c.151-12A>C
NM_000363.5(TNNI3):c.151-6C>G rs377258542
NM_000363.5(TNNI3):c.156G>A (p.Leu52=)
NM_000363.5(TNNI3):c.157C>T (p.Leu53=) rs763981651
NM_000363.5(TNNI3):c.207C>G (p.Arg69=) rs201422579
NM_000363.5(TNNI3):c.226C>T (p.Leu76=)
NM_000363.5(TNNI3):c.24+6A>G
NM_000363.5(TNNI3):c.246G>T (p.Pro82=) rs397516343
NM_000363.5(TNNI3):c.277C>T (p.Leu93=)
NM_000363.5(TNNI3):c.279G>A (p.Leu93=) rs1568859087
NM_000363.5(TNNI3):c.283-13G>T
NM_000363.5(TNNI3):c.283-9C>T rs759922995
NM_000363.5(TNNI3):c.28A>G (p.Arg10Gly)
NM_000363.5(TNNI3):c.294A>G (p.Arg98=) rs1568858567
NM_000363.5(TNNI3):c.303C>T (p.His101=) rs199539066
NM_000363.5(TNNI3):c.318G>A (p.Lys106=) rs750350912
NM_000363.5(TNNI3):c.330G>A (p.Glu110=)
NM_000363.5(TNNI3):c.336C>T (p.Tyr112=) rs559450042
NM_000363.5(TNNI3):c.340A>G (p.Ile114Val) rs730881070
NM_000363.5(TNNI3):c.354C>T (p.Val118=)
NM_000363.5(TNNI3):c.373-14del
NM_000363.5(TNNI3):c.373-4C>G rs2288530
NM_000363.5(TNNI3):c.373-8G>A rs369244036
NM_000363.5(TNNI3):c.384G>A (p.Leu128=) rs373130533
NM_000363.5(TNNI3):c.39C>G (p.Arg13=) rs397516346
NM_000363.5(TNNI3):c.402C>T (p.Asp134=)
NM_000363.5(TNNI3):c.432G>C (p.Leu144=)
NM_000363.5(TNNI3):c.432G>T (p.Leu144=) rs776615304
NM_000363.5(TNNI3):c.471G>A (p.Ala157=) rs747756509
NM_000363.5(TNNI3):c.474G>C (p.Leu158=) rs749880457
NM_000363.5(TNNI3):c.508C>A (p.Arg170=)
NM_000363.5(TNNI3):c.516C>T (p.His172=)
NM_000363.5(TNNI3):c.522G>A (p.Lys174=)
NM_000363.5(TNNI3):c.550-12G>A
NM_000363.5(TNNI3):c.550-13C>T
NM_000363.5(TNNI3):c.550-14T>C
NM_000363.5(TNNI3):c.55A>G (p.Ile19Val) rs755862334
NM_000363.5(TNNI3):c.567A>G (p.Gly189=) rs902161211
NM_000363.5(TNNI3):c.585C>T (p.Ile195=)
NM_000363.5(TNNI3):c.606G>A (p.Glu202=) rs796474405
NM_000363.5(TNNI3):c.612C>G (p.Arg204=)
NM_000363.5(TNNI3):c.6G>A (p.Ala2=) rs397516361
NM_000363.5(TNNI3):c.9T>C (p.Asp3=)

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