"PreventionGenetics, part of Exact Sciences"[submitter] AND "NDUFS3"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 618750	NM_004551.3(NDUFS3):c.99G>T (p.Pro33=)	NDUFS3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 214802	NM_004551.3(NDUFS3):c.475G>C (p.Val159Leu)	NDUFS3 (V159L)	Single nucleotide variant (missense variant)	Mitochondrial complex I deficiency, nuclear type 1 +3 more	GConflicting classifications of pathogenicity
Select item 2806992	NM_004551.3(NDUFS3):c.732C>T (p.Val244=)	NDUFS3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1360225	NM_004551.3(NDUFS3):c.736C>T (p.Arg246Cys)	NDUFS3 (R246C)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 732328	NM_004551.3(NDUFS3):c.768C>T (p.Ala256=)	NDUFS3	Single nucleotide variant (synonymous variant)	NDUFS3-related disorder +1 more	GLikely benign
Select item 304999	NM_004551.3(NDUFS3):c.783T>C (p.Pro261=)	NDUFS3	Single nucleotide variant (synonymous variant)	Mitochondrial complex I deficiency, nuclear type 1 +3 more	GConflicting classifications of pathogenicity

ClinVar