"Ambry Genetics"[submitter] AND "LOC130004379"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2237161	NM_001134658.3(SLC35G1):c.44C>T (p.Pro15Leu)	LOC130004379, SLC35G1 (P15L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2207817	NM_001134658.3(SLC35G1):c.55C>A (p.Leu19Ile)	LOC130004379, SLC35G1 (L19I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2397437	NM_001134658.3(SLC35G1):c.77G>T (p.Gly26Val)	LOC130004379, SLC35G1 (G26V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2613110	NM_001134658.3(SLC35G1):c.109G>C (p.Ala37Pro)	LOC130004379, SLC35G1 (A37P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2347820	NM_001134658.3(SLC35G1):c.132G>T (p.Arg44Ser)	LOC130004379, SLC35G1 (R44S)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2231399	NM_001134658.3(SLC35G1):c.152C>T (p.Ser51Leu)	LOC130004379, SLC35G1 (S51L)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance

ClinVar