"GeneDx"[submitter] AND "COX8A"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1317858	NC_000011.10:g.63974419G>A	COX8A	Single nucleotide variant	not provided	GLikely benign
Select item 673121	NM_004074.3(COX8A):c.22C>T (p.Leu8=)	COX8A, LOC130005904	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 771443	NM_004074.3(COX8A):c.67C>T (p.Arg23Cys)	COX8A, LOC130005904 (R23C)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 709505	NM_004074.3(COX8A):c.111C>A (p.Ile37=)	COX8A, LOC130005904	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 683606	NM_004074.3(COX8A):c.114+287T>G	COX8A	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1318076	NM_004074.3(COX8A):c.115-277A>C	COX8A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 683608	NM_004074.3(COX8A):c.115-277A>G	COX8A	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar