"GeneDx"[submitter] AND "COA7"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58079	GRCh38/hg38 1p32.3-31.1(chr1:52595352-76767765)x3	ACADM, ACOT11 +570 more	Copy number gain	See cases	GPathogenic
Select item 1287335	NM_023077.3(COA7):c.656A>G (p.Lys219Arg)	COA7 (K219R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1281780	NM_023077.3(COA7):c.248-36C>G	COA7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253097	NM_023077.3(COA7):c.248-92dup	COA7	Duplication (intron variant)	not provided	GBenign
Select item 1271736	NM_023077.3(COA7):c.248-145C>T	COA7	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259726	NC_000001.11:g.52698478G>T	COA7	Single nucleotide variant	not provided	GBenign
Select item 1258438	NC_000001.11:g.52698548C>T	COA7, LOC129930555	Single nucleotide variant	not provided	GBenign

ClinVar