"Fulgent Genetics, Fulgent Genetics"[submitter] AND "TNNI3K"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1599675	NM_015978.3(TNNI3K):c.193G>T (p.Glu65Ter)	FPGT-TNNI3K, TNNI3K (E166* +1 more)	Single nucleotide variant (nonsense)	not provided +1 more	GBenign/Likely benign
Select item 626247	NM_015978.3(TNNI3K):c.2302G>A (p.Glu768Lys)	FPGT-TNNI3K, LRRC53 +1 more (E768K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic/Likely pathogenic