"Ambry Genetics"[submitter] AND "LOC130006235"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3186705	NM_030930.4(UNC93B1):c.226G>C (p.Gly76Arg)	LOC130006235, UNC93B1 (G76R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2110346	NM_030930.4(UNC93B1):c.214A>G (p.Met72Val)	LOC130006235, UNC93B1 (M72V)	Single nucleotide variant (missense variant)	Herpes simplex encephalitis, susceptibility to, 1 +1 more	GUncertain significance
Select item 654962	NM_030930.4(UNC93B1):c.193C>G (p.Leu65Val)	LOC130006235, UNC93B1 (L65V)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 844807	NM_030930.4(UNC93B1):c.151C>G (p.Arg51Gly)	UNC93B1, LOC130006235 (R51G)	Single nucleotide variant (missense variant)	Herpes simplex encephalitis, susceptibility to, 1 +1 more	GUncertain significance
Select item 626042	NM_030930.4(UNC93B1):c.148C>A (p.Arg50Ser)	LOC130006235, UNC93B1 (R50S)	Single nucleotide variant (missense variant)	Herpes simplex encephalitis, susceptibility to, 1 +1 more	GUncertain significance
Select item 1022414	NM_030930.4(UNC93B1):c.136G>A (p.Glu46Lys)	LOC130006235, UNC93B1 (E46K)	Single nucleotide variant (missense variant)	Herpes simplex encephalitis, susceptibility to, 1 +1 more	GUncertain significance

ClinVar