"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "COG2"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 709599	NM_007357.3(COG2):c.183C>T (p.Val61=)	COG2	Single nucleotide variant (synonymous variant)	Congenital disorder of glycosylation, type IIq +1 more	GBenign
Select item 774284	NM_007357.3(COG2):c.708G>A (p.Thr236=)	COG2	Single nucleotide variant (synonymous variant)	Congenital disorder of glycosylation, type IIq +1 more	GBenign/Likely benign
Select item 478370	NM_007357.3(COG2):c.1014T>C (p.Asp338=)	COG2	Single nucleotide variant (synonymous variant)	Congenital disorder of glycosylation, type IIq +2 more	GBenign/Likely benign
Select item 806379	NM_007357.3(COG2):c.1066C>T (p.Arg356Trp)	COG2 (R356W)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1176856	NM_007357.3(COG2):c.1089T>C (p.Ser363=)	COG2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 806380	NM_007357.3(COG2):c.1825G>A (p.Asp609Asn)	COG2 (D609N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 715155	NM_007357.3(COG2):c.2061C>T (p.Asp687=)	COG2	Single nucleotide variant (synonymous variant)	Congenital disorder of glycosylation, type IIq +1 more	GLikely benign

ClinVar