"Center for Human Genetics, University of Leuven"[submitter] AND "TNNI - 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 43395	NM_000363.5(TNNI3):c.557G>A (p.Arg186Gln)	TNNI3 (R186Q)	Single nucleotide variant (missense variant)	Primary familial hypertrophic cardiomyopathy +5 more	GPathogenic/Likely pathogenic
Select item 179285	NM_000363.5(TNNI3):c.508C>T (p.Arg170Trp)	TNNI3 (R170W)	Single nucleotide variant (missense variant)	Restrictive cardiomyopathy +3 more	GPathogenic/Likely pathogenic
Select item 43384	NM_000363.5(TNNI3):c.434G>A (p.Arg145Gln)	TNNI3 (R145Q)	Single nucleotide variant (missense variant)	Primary familial hypertrophic cardiomyopathy +8 more	GPathogenic/Likely pathogenic
Select item 12426	NM_000363.5(TNNI3):c.433C>T (p.Arg145Trp)	TNNI3 (R145W)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +3 more	GPathogenic
Select item 427955	NM_000363.5(TNNI3):c.298C>T (p.Leu100Phe)	TNNI3 (L100F)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +2 more	GUncertain significance

ClinVar