"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "TNNI3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 177679	NM_000363.5(TNNI3):c.611G>A (p.Arg204His)	TNNI3 (R204H)	Single nucleotide variant (missense variant)	Cardiomyopathy +4 more	GPathogenic/Likely pathogenic
Select item 36883	NM_000363.5(TNNI3):c.562G>A (p.Val188Met)	TNNI3 (V188M)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +3 more	GConflicting classifications of pathogenicity
Select item 177630	NM_000363.5(TNNI3):c.497C>T (p.Ser166Phe)	TNNI3 (S166F)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +4 more	GPathogenic/Likely pathogenic
Select item 43389	NM_000363.5(TNNI3):c.485G>A (p.Arg162Gln)	TNNI3 (R162Q)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +8 more	GPathogenic/Likely pathogenic
Select item 1163636	NM_000363.5(TNNI3):c.386C>T (p.Thr129Ile)	TNNI3 (T129I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 181575	NM_000363.5(TNNI3):c.292C>T (p.Arg98Ter)	TNNI3 (R98*)	Single nucleotide variant (nonsense)	not provided +7 more	GConflicting classifications of pathogenicity

ClinVar