"Ambry Genetics"[submitter] AND "LOC126863145"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3328987	NM_001039141.3(TRIOBP):c.5383C>T (p.Pro1795Ser)	LOC126863145, TRIOBP (P82S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2474998	NM_001039141.3(TRIOBP):c.5410A>G (p.Thr1804Ala)	LOC126863145, TRIOBP (T1804A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2203248	NM_001039141.3(TRIOBP):c.5416C>G (p.Gln1806Glu)	LOC126863145, TRIOBP (Q93E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3328989	NM_001039141.3(TRIOBP):c.5525G>C (p.Cys1842Ser)	LOC126863145, TRIOBP (C1842S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 229360	NM_001039141.3(TRIOBP):c.5528C>T (p.Thr1843Met)	LOC126863145, TRIOBP (T1843M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2317577	NM_001039141.3(TRIOBP):c.5561A>G (p.Tyr1854Cys)	LOC126863145, TRIOBP (Y141C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar