"Fulgent Genetics, Fulgent Genetics"[submitter] AND "DOCK6"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1414519	NM_020812.4(DOCK6):c.4198G>A (p.Val1400Met)	DOCK6, DOCK6-AS1 (V1435M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 1319695	NM_020812.4(DOCK6):c.4012C>T (p.Arg1338Ter)	DOCK6, DOCK6-AS1 (R1338* +1 more)	Single nucleotide variant (nonsense)	Adams-Oliver syndrome 2 +1 more	GPathogenic/Likely pathogenic
Select item 445548	NM_020812.4(DOCK6):c.3913C>T (p.Arg1305Cys)	DOCK6, DOCK6-AS1 (R1305C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1174644	NM_020812.4(DOCK6):c.2629C>T (p.Arg877Cys)	DOCK6 (R877C)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 737455	NM_020812.4(DOCK6):c.2505C>T (p.Tyr835=)	DOCK6	Single nucleotide variant (synonymous variant)	Adams-Oliver syndrome 2 +1 more	GLikely benign
Select item 1641623	NM_020812.4(DOCK6):c.1833-19C>G	DOCK6	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 771212	NM_020812.4(DOCK6):c.1289G>A (p.Arg430His)	DOCK6 (R430H)	Single nucleotide variant (missense variant)	Adams-Oliver syndrome 2 +1 more	GLikely benign
Select item 771213	NM_020812.4(DOCK6):c.885C>T (p.Asn295=)	DOCK6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign

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