"Ambry Genetics"[submitter] AND "ARL9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2352948	NM_001363794.2(ARL9):c.507C>G (p.Ile169Met)	ARL9 (I169M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129593	NM_001363794.2(ARL9):c.610A>G (p.Asn204Asp)	ARL9 (N45D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129594	NM_001363794.2(ARL9):c.629C>A (p.Ala210Glu)	ARL9 (A210E +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129595	NM_001363794.2(ARL9):c.632C>T (p.Ala211Val)	ARL9 (A42V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129596	NM_001363794.2(ARL9):c.740C>T (p.Pro247Leu)	ARL9 (P247L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306545	NM_001363794.2(ARL9):c.740C>G (p.Pro247Arg)	ARL9 (P105R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317616	NM_001363794.2(ARL9):c.778C>G (p.Leu260Val)	ARL9 (L147V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar