"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 931244	NM_015570.4(AUTS2):c.607C>T (p.Arg203Trp)	AUTS2 (R203W)	Single nucleotide variant (missense variant)	Autism spectrum disorder due to AUTS2 deficiency	GUncertain significance
Select item 546070	NM_015570.4(AUTS2):c.742+1G>A	AUTS2	Single nucleotide variant (splice donor variant)	not provided +1 more	GPathogenic
Select item 931890	NM_015570.4(AUTS2):c.932C>G (p.Thr311Arg)	AUTS2 (T311R)	Single nucleotide variant (missense variant)	Autism spectrum disorder due to AUTS2 deficiency	GUncertain significance
Select item 374065	NM_015570.4(AUTS2):c.3377ACC[9] (p.His1133dup)	AUTS2	Microsatellite (inframe_insertion)	Autism +3 more	GConflicting classifications of pathogenicity
Select item 930760	NM_015570.4(AUTS2):c.3632C>A (p.Thr1211Asn)	AUTS2 (T1187N +1 more)	Single nucleotide variant (missense variant)	Autism spectrum disorder due to AUTS2 deficiency	GUncertain significance
Select item 930612	NM_015570.4(AUTS2):c.3707G>A (p.Arg1236Lys)	AUTS2 (R1236K +1 more)	Single nucleotide variant (missense variant)	Autism spectrum disorder due to AUTS2 deficiency +1 more	GUncertain significance

ClinVar