"Ambry Genetics"[submitter] AND "SARM1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2350109	NM_015077.4(SARM1):c.25G>C (p.Ala9Pro)	SARM1 (A9P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389459	NM_015077.4(SARM1):c.49G>C (p.Ala17Pro)	LOC130060546, SARM1 (A17P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333717	NM_080669.6(SLC46A1):c.1274C>T (p.Pro425Leu)	SARM1, SLC46A1 (P397L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3067702	NM_080669.6(SLC46A1):c.1205C>T (p.Ala402Val)	SARM1, SLC46A1 (A374V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2401032	NM_080669.6(SLC46A1):c.1187C>A (p.Ala396Asp)	SARM1, SLC46A1 (A396D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 850	NM_080669.6(SLC46A1):c.1082-1G>A	SLC46A1, SARM1	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases +2 more	GPathogenic

ClinVar