C4748796[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2434080	NM_004544.4(NDUFA10):c.1025_1026insATGG (p.Tyr343fs)	NDUFA10 (G306fs +1 more)	Insertion (frameshift variant +1 more)	Mitochondrial complex 1 deficiency, nuclear type 22	GUncertain significance
Select item 632354	NM_004544.4(NDUFA10):c.604dup (p.His202fs)	NDUFA10 (H202fs)	Duplication (frameshift variant +1 more)	Mitochondrial complex 1 deficiency, nuclear type 22 +1 more	GConflicting classifications of pathogenicity