"Ambry Genetics"[submitter] AND "DACT3-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2527609	NM_145056.3(DACT3):c.236T>G (p.Leu79Arg)	DACT3, DACT3-AS1 (L79R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2244138	NM_145056.3(DACT3):c.92A>G (p.His31Arg)	DACT3, DACT3-AS1 (H31R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2305005	NM_016457.5(PRKD2):c.2620C>T (p.Arg874Cys)	PRKD2, DACT3-AS1 (R717C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2286760	NM_016457.5(PRKD2):c.2494A>G (p.Ser832Gly)	DACT3-AS1, PRKD2 (S675G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2394239	NM_016457.5(PRKD2):c.2354A>G (p.Asn785Ser)	PRKD2, DACT3-AS1 (N628S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2218992	NM_016457.5(PRKD2):c.2342T>C (p.Ile781Thr)	PRKD2, DACT3-AS1 (I624T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar