ClinVar Miner

List of variants in gene TNNI3 studied for Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome

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Total variants: 25
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HGVS dbSNP
NM_000363.4(TNNI3):c.-148A>G rs73935313
NM_000363.5(TNNI3):c.*35C>T rs375447438
NM_000363.5(TNNI3):c.*44A>G
NM_000363.5(TNNI3):c.-103C>T rs557391836
NM_000363.5(TNNI3):c.-133G>T rs886054636
NM_000363.5(TNNI3):c.-45C>T
NM_000363.5(TNNI3):c.-47C>T rs202159627
NM_000363.5(TNNI3):c.-85A>C rs186540595
NM_000363.5(TNNI3):c.-98C>A
NM_000363.5(TNNI3):c.104C>A (p.Ala35Asp)
NM_000363.5(TNNI3):c.109-15A>G rs779144176
NM_000363.5(TNNI3):c.12-7del rs370714315
NM_000363.5(TNNI3):c.139T>C (p.Leu47=) rs587780967
NM_000363.5(TNNI3):c.151-6C>G rs377258542
NM_000363.5(TNNI3):c.157C>T (p.Leu53=) rs763981651
NM_000363.5(TNNI3):c.198G>A (p.Glu66=) rs3729710
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.273G>A (p.Ala91=) rs75491697
NM_000363.5(TNNI3):c.283-9C>T rs759922995
NM_000363.5(TNNI3):c.372+7C>T rs367809676
NM_000363.5(TNNI3):c.373-15C>G rs192630178
NM_000363.5(TNNI3):c.373-4C>G rs2288530
NM_000363.5(TNNI3):c.466C>G (p.Gln156Glu)
NM_000363.5(TNNI3):c.550-11C>T rs886054635

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