ClinVar Miner

List of variants in gene TNNI3 reported as likely benign for Hypertrophic cardiomyopathy

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Total variants: 55
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HGVS dbSNP
NM_000363.4(TNNI3):c.-148A>G rs73935313
NM_000363.5(TNNI3):c.108+10G>A
NM_000363.5(TNNI3):c.108+8G>C
NM_000363.5(TNNI3):c.108+8G>T
NM_000363.5(TNNI3):c.12-8C>T
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.150+7A>G
NM_000363.5(TNNI3):c.150+9G>T rs750675608
NM_000363.5(TNNI3):c.151-6C>G rs377258542
NM_000363.5(TNNI3):c.156G>A (p.Leu52=)
NM_000363.5(TNNI3):c.160C>T (p.Leu54=) rs1555864068
NM_000363.5(TNNI3):c.198G>A (p.Glu66=) rs3729710
NM_000363.5(TNNI3):c.207C>G (p.Arg69=) rs201422579
NM_000363.5(TNNI3):c.213G>A (p.Glu71=)
NM_000363.5(TNNI3):c.235C>T (p.Arg79Cys) rs3729712
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser) rs77615401
NM_000363.5(TNNI3):c.246G>A (p.Pro82=) rs397516343
NM_000363.5(TNNI3):c.25-7A>C
NM_000363.5(TNNI3):c.258C>G (p.Ala86=) rs727503508
NM_000363.5(TNNI3):c.264G>T (p.Leu88=) rs772928416
NM_000363.5(TNNI3):c.282+10C>G rs974607293
NM_000363.5(TNNI3):c.283-9C>T rs759922995
NM_000363.5(TNNI3):c.294A>G (p.Arg98=) rs1568858567
NM_000363.5(TNNI3):c.300C>G (p.Leu100=)
NM_000363.5(TNNI3):c.303C>T (p.His101=) rs199539066
NM_000363.5(TNNI3):c.315C>T (p.Asp105=) rs1555863727
NM_000363.5(TNNI3):c.336C>T (p.Tyr112=) rs559450042
NM_000363.5(TNNI3):c.363C>T (p.Asn121=) rs371490136
NM_000363.5(TNNI3):c.369G>A (p.Thr123=)
NM_000363.5(TNNI3):c.372+7C>T rs367809676
NM_000363.5(TNNI3):c.372+8G>A rs200573982
NM_000363.5(TNNI3):c.372+8G>T rs200573982
NM_000363.5(TNNI3):c.373-4C>G rs2288530
NM_000363.5(TNNI3):c.373-8G>A rs369244036
NM_000363.5(TNNI3):c.373-8G>C 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.432G>T (p.Leu144=) rs776615304
NM_000363.5(TNNI3):c.45A>C (p.Ala15=) rs377421427
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.495G>A (p.Glu165=) rs1333619884
NM_000363.5(TNNI3):c.516C>T (p.His172=)
NM_000363.5(TNNI3):c.51C>G (p.Ala17=)
NM_000363.5(TNNI3):c.543C>G (p.Thr181=)
NM_000363.5(TNNI3):c.546G>A (p.Glu182=)
NM_000363.5(TNNI3):c.57C>T (p.Ile19=) rs778133452
NM_000363.5(TNNI3):c.585C>T (p.Ile195=)
NM_000363.5(TNNI3):c.606G>A (p.Glu202=) rs796474405
NM_000363.5(TNNI3):c.609C>T (p.Gly203=) rs587780968
NM_000363.5(TNNI3):c.63C>G (p.Arg21=) rs1555864377
NM_000363.5(TNNI3):c.6G>A (p.Ala2=) rs397516361
NM_000363.5(TNNI3):c.84T>C (p.Ala28=)
NM_000363.5(TNNI3):c.93G>C (p.Thr31=)

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