ClinVar Miner

List of variants in gene TNNI3 reported as uncertain significance for Familial hypertrophic cardiomyopathy 7

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Total variants: 15
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HGVS dbSNP
NM_000363.5(TNNI3):c.*44A>G
NM_000363.5(TNNI3):c.-45C>T
NM_000363.5(TNNI3):c.104C>A (p.Ala35Asp)
NM_000363.5(TNNI3):c.109-15A>G rs779144176
NM_000363.5(TNNI3):c.139T>C (p.Leu47=) rs587780967
NM_000363.5(TNNI3):c.151-6C>G rs377258542
NM_000363.5(TNNI3):c.206G>A (p.Arg69His)
NM_000363.5(TNNI3):c.283-9C>T rs759922995
NM_000363.5(TNNI3):c.347C>G (p.Ala116Gly) rs777177571
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
NM_000363.5(TNNI3):c.596G>A (p.Ser199Asn) rs730881091

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