"Ambry Genetics"[submitter] AND "PCDH9-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2278952	NM_203487.3(PCDH9):c.3634A>G (p.Thr1212Ala)	PCDH9, PCDH9-AS1 (T1136A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293386	NM_203487.3(PCDH9):c.3553G>C (p.Glu1185Gln)	PCDH9, PCDH9-AS1 (E1143Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209262	NM_203487.3(PCDH9):c.3511G>C (p.Asp1171His)	PCDH9, PCDH9-AS1 (D1137H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262685	NM_203487.3(PCDH9):c.3505A>G (p.Lys1169Glu)	PCDH9, PCDH9-AS1 (K1127E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479630	NM_203487.3(PCDH9):c.3488C>T (p.Pro1163Leu)	PCDH9, PCDH9-AS1 (P1087L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384065	NM_203487.3(PCDH9):c.3482T>G (p.Phe1161Cys)	PCDH9, PCDH9-AS1 (F1127C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3209261	NM_203487.3(PCDH9):c.3461C>T (p.Pro1154Leu)	PCDH9, PCDH9-AS1 (P1154L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar