Related gene-specific medical variations for Gene (Select 29844) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3325647	NM_013342.4(TFPT):c.668T>C (p.Phe223Ser)	NDUFA3, TFPT (F223S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299653	NM_013342.4(TFPT):c.716A>G (p.Asp239Gly)	NDUFA3, TFPT (D230G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance