"Fulgent Genetics, Fulgent Genetics"[submitter] AND "NDUFB9"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1318387	NM_005005.3(NDUFB9):c.-51A>G	NDUFB9	Single nucleotide variant (5 prime UTR variant)	Mitochondrial complex 1 deficiency, nuclear type 24 +1 more	GLikely benign
Select item 138472	NM_005005.3(NDUFB9):c.24C>T (p.Pro8=)	NDUFB9	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +2 more	GBenign/Likely benign