"Ambry Genetics"[submitter] AND "LOC126862363"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3281993	NM_002080.4(GOT2):c.689C>T (p.Ala230Val)	GOT2, LOC126862363 (A230V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321606	NM_002080.4(GOT2):c.670G>A (p.Glu224Lys)	GOT2, LOC126862363 (E224K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332708	NM_002080.4(GOT2):c.650C>A (p.Thr217Lys)	GOT2, LOC126862363 (T174K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268900	NM_002080.4(GOT2):c.602T>C (p.Ile201Thr)	GOT2, LOC126862363 (I201T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383391	NM_002080.4(GOT2):c.584T>C (p.Val195Ala)	GOT2, LOC126862363 (V195A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281992	NM_002080.4(GOT2):c.478C>T (p.Pro160Ser)	GOT2, LOC126862363 (P117S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar