"Ambry Genetics"[submitter] AND "ADAMTS9-AS2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1349467	NM_182920.2(ADAMTS9):c.422C>A (p.Ser141Tyr)	ADAMTS9, ADAMTS9-AS2 (S141Y)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3268017	NM_182920.2(ADAMTS9):c.316G>A (p.Gly106Ser)	ADAMTS9, ADAMTS9-AS2 (G106S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078555	NM_182920.2(ADAMTS9):c.253G>A (p.Ala85Thr)	ADAMTS9, ADAMTS9-AS2 (A85T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343411	NM_182920.2(ADAMTS9):c.199G>T (p.Val67Phe)	ADAMTS9, ADAMTS9-AS2 (V67F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594432	NM_182920.2(ADAMTS9):c.182A>T (p.Glu61Val)	ADAMTS9, ADAMTS9-AS2 (E61V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229001	NM_182920.2(ADAMTS9):c.129G>T (p.Glu43Asp)	ADAMTS9, ADAMTS9-AS2 (E43D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298693	NM_182920.2(ADAMTS9):c.85G>A (p.Val29Met)	ADAMTS9, ADAMTS9-AS2 (V29M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078683	NM_182920.2(ADAMTS9):c.46G>A (p.Asp16Asn)	ADAMTS9, ADAMTS9-AS2 (D16N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar