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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 706096	NM_001012301.4(ARSI):c.1302C>T (p.Gly434=)	ARSI	Single nucleotide variant (synonymous variant)	ARSI-related disorder +1 more	GLikely benign
Select item 465194	NM_001012301.4(ARSI):c.1242C>T (p.Ala414=)	ARSI	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1980520	NM_001012301.4(ARSI):c.1007G>A (p.Arg336Gln)	ARSI (R336Q)	Single nucleotide variant (missense variant)	Spastic paraplegia +1 more	GBenign/Likely benign
Select item 703924	NM_001012301.4(ARSI):c.930G>A (p.Pro310=)	ARSI	Single nucleotide variant (synonymous variant)	ARSI-related disorder +1 more	GLikely benign
Select item 465199	NM_001012301.4(ARSI):c.894T>C (p.Asn298=)	ARSI	Single nucleotide variant (synonymous variant)	ARSI-related disorder +1 more	GBenign
Select item 971595	NM_001012301.4(ARSI):c.613G>A (p.Gly205Ser)	ARSI (G205S)	Single nucleotide variant (missense variant)	Spastic paraplegia +1 more	GUncertain significance
Select item 3013263	NM_001012301.4(ARSI):c.573C>T (p.Phe191=)	ARSI	Single nucleotide variant (synonymous variant)	Spastic paraplegia +1 more	GLikely benign
Select item 3050253	NM_001012301.4(ARSI):c.123C>T (p.Ala41=)	ARSI	Single nucleotide variant (synonymous variant)	ARSI-related disorder	GLikely benign

ClinVar