"PreventionGenetics, part of Exact Sciences"[submitter] AND "COA6"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058720	NM_001206641.3(COA6):c.45G>A (p.Val15=)	COA6, COA6-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	COA6-related disorder	GLikely benign
Select item 506753	NM_001206641.3(COA6):c.191C>G (p.Ala64Gly)	COA6 (A64G)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 3048883	NM_001206641.3(COA6):c.330G>A (p.Lys110=)	COA6	Single nucleotide variant (synonymous variant)	COA6-related disorder	GLikely benign

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