"Ambry Genetics"[submitter] AND "DOCK8-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3085118	NR_160804.1(DOCK8-AS1):n.1145T>G	DOCK8, DOCK8-AS1	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3085117	NR_160804.1(DOCK8-AS1):n.1003G>A	DOCK8, DOCK8-AS1 +1 more	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3085116	NR_160804.1(DOCK8-AS1):n.943A>T	DOCK8, DOCK8-AS1 +1 more	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3085115	NM_203447.4(DOCK8):c.-106C>G	DOCK8, DOCK8-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 429234	NM_203447.4(DOCK8):c.52A>G (p.Arg18Gly)	DOCK8, DOCK8-AS1 +1 more (R18G)	Single nucleotide variant (non-coding transcript variant +1 more)	Autosomal recessive hyper-IgE syndrome +2 more	GConflicting classifications of pathogenicity
Select item 3085114	NM_203447.4(DOCK8):c.53+13C>G	DOCK8, DOCK8-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3085119	NM_203447.4(DOCK8):c.53+361G>A	DOCK8, DOCK8-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

ClinVar