"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "FPGT-TNNI3K"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1978656	NM_015978.3(TNNI3K):c.997A>G (p.Ile333Val)	FPGT-TNNI3K, TNNI3K (I333V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1380594	NM_015978.3(TNNI3K):c.1172A>G (p.Glu391Gly)	FPGT-TNNI3K, TNNI3K (E492G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2180971	NM_015978.3(TNNI3K):c.1389T>G (p.Ile463Met)	FPGT-TNNI3K, TNNI3K (I463M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 1590549	NM_015978.3(TNNI3K):c.1550A>G (p.Asn517Ser)	FPGT-TNNI3K, TNNI3K (N517S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1545733	NM_015978.3(TNNI3K):c.1772G>C (p.Ser591Thr)	FPGT-TNNI3K, TNNI3K (S591T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1448933	NM_015978.3(TNNI3K):c.2033C>A (p.Ala678Asp)	FPGT-TNNI3K, TNNI3K (A779D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar