GOLGA6L22[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145030	GRCh38/hg38 15q11.2(chr15:22358243-22544169)x3	GOLGA6L22	Copy number gain	See cases	GBenign
Select item 2644966	NM_001396956.1(GOLGA6L22):c.231C>T (p.Ser77=)	GOLGA6L22	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644965	NM_001396956.1(GOLGA6L22):c.1396G>T (p.Glu466Ter)	GOLGA6L22 (E465* +1 more)	Single nucleotide variant (nonsense)	not provided	GLikely benign
Select item 2644964	NM_001396956.1(GOLGA6L22):c.1519C>A (p.Arg507=)	GOLGA6L22	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644963	NM_001396956.1(GOLGA6L22):c.1991A>G (p.Glu664Gly)	GOLGA6L22 (E663G +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2644962	NM_001396956.1(GOLGA6L22):c.2112G>A (p.Met704Ile)	GOLGA6L22 (M703I +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2644961	NM_001396956.1(GOLGA6L22):c.2113G>A (p.Gly705Arg)	GOLGA6L22 (G704R +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign

ClinVar