"PreventionGenetics, part of Exact Sciences"[submitter] AND "COX6A2"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3045482	NM_005205.4(COX6A2):c.255C>T (p.Ser85=)	COX6A2	Single nucleotide variant (synonymous variant)	COX6A2-related disorder	GLikely benign
Select item 3059761	NM_005205.4(COX6A2):c.219C>T (p.Pro73=)	COX6A2	Single nucleotide variant (synonymous variant)	COX6A2-related disorder	GBenign
Select item 2646480	NM_005205.4(COX6A2):c.34T>G (p.Leu12Val)	COX6A2 (L12V)	Single nucleotide variant (missense variant)	COX6A2-related disorder +1 more	GBenign/Likely benign

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