"Fulgent Genetics, Fulgent Genetics"[submitter] AND "COX15"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 298420	NM_078470.6(COX15):c.131G>A (p.Ser44Asn)	COX15 (S44N)	Single nucleotide variant (missense variant +2 more)	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 +3 more	GUncertain significance
Select item 298424	NM_004376.7(COX15):c.-84G>A	COX15	Single nucleotide variant	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 +1 more	GUncertain significance