"GeneDx"[submitter] AND "COQ7-DT"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1267344	NC_000016.10:g.19067281del	COQ7, COQ7-DT	Deletion	not provided	GBenign
Select item 669474	NM_016138.4(COQ7):c.-357A>T	COQ7, COQ7-DT	Single nucleotide variant	not provided	GBenign
Select item 1316957	NC_000016.10:g.19067449T>C	COQ7-DT, COQ7	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 1316734	NC_000016.10:g.19067503G>T	COQ7, COQ7-DT	Single nucleotide variant	not provided	GLikely benign
Select item 1316733	NC_000016.10:g.19067610G>A	COQ7, COQ7-DT	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 1282807	NM_016138.5(COQ7):c.15GGC[5] (p.Ala9dup)	COQ7, COQ7-DT +1 more	Microsatellite (inframe_insertion +1 more)	not provided	GBenign

ClinVar