"PreventionGenetics, part of Exact Sciences"[submitter] AND "ARSF"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042994	NM_001201539.2(ARSF):c.165G>A (p.Thr55=)	ARSF	Single nucleotide variant (synonymous variant)	ARSF-related disorder	GLikely benign
Select item 3041701	NM_001201539.2(ARSF):c.535C>T (p.Arg179Cys)	ARSF (R179C)	Single nucleotide variant (missense variant)	ARSF-related disorder	GLikely benign
Select item 3041570	NM_001201539.2(ARSF):c.689G>A (p.Gly230Asp)	ARSF (G230D)	Single nucleotide variant (missense variant)	ARSF-related disorder	GBenign
Select item 3040847	NM_001201539.2(ARSF):c.716C>A (p.Ser239Tyr)	ARSF (S239Y)	Single nucleotide variant (missense variant)	ARSF-related disorder	GLikely benign
Select item 3043061	NM_001201539.2(ARSF):c.1004G>A (p.Arg335Lys)	ARSF (R335K)	Single nucleotide variant (missense variant)	ARSF-related disorder	GBenign
Select item 771943	NM_001201539.2(ARSF):c.1102+5G>A	ARSF	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 3041861	NM_001201539.2(ARSF):c.1443T>A (p.Ala481=)	ARSF	Single nucleotide variant (synonymous variant)	ARSF-related disorder	GLikely benign
Select item 2659874	NM_001201539.2(ARSF):c.1689G>A (p.Lys563=)	ARSF	Single nucleotide variant (synonymous variant)	ARSF-related disorder +1 more	GLikely benign

ClinVar