"Diagnostic Laboratory, Department of Genetics, University Medical Cen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 518283	NM_020812.4(DOCK6):c.4959C>T (p.Asn1653=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	Adams-Oliver syndrome 2 +1 more	GBenign
Select item 518284	NM_020812.4(DOCK6):c.4895C>T (p.Ala1632Val)	DOCK6, DOCK6-AS1 (A1632V +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1174785	NM_020812.4(DOCK6):c.4751+1G>A	DOCK6, DOCK6-AS1	Single nucleotide variant (splice donor variant)	not provided	GPathogenic
Select item 1174753	NM_020812.4(DOCK6):c.4343C>T (p.Pro1448Leu)	DOCK6, DOCK6-AS1 (P1448L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 518285	NM_020812.4(DOCK6):c.4050T>C (p.Asn1350=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	Adams-Oliver syndrome 2 +1 more	GBenign
Select item 518286	NM_020812.4(DOCK6):c.4044G>A (p.Pro1348=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	Adams-Oliver syndrome 2 +1 more	GBenign
Select item 518287	NM_020812.4(DOCK6):c.3894+19G>A	DOCK6, DOCK6-AS1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 518288	NM_020812.4(DOCK6):c.3876A>G (p.Leu1292=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 518289	NM_020812.4(DOCK6):c.3858T>C (p.Asp1286=)	DOCK6, DOCK6-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign

ClinVar