"Ambry Genetics"[submitter] AND "TPD52L1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2606908	NM_003287.4(TPD52L1):c.89T>C (p.Met30Thr)	TPD52L1 (M1T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2271602	NM_003287.4(TPD52L1):c.198G>C (p.Glu66Asp)	TPD52L1 (E66D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515005	NM_003287.4(TPD52L1):c.347A>G (p.Asn116Ser)	TPD52L1 (N116S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181514	NM_003287.4(TPD52L1):c.499G>A (p.Gly167Ser)	TPD52L1 (G167S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519644	NM_003287.4(TPD52L1):c.503C>T (p.Thr168Met)	TPD52L1 (T173M +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181515	NM_003287.4(TPD52L1):c.535C>G (p.Leu179Val)	TPD52L1 (L150V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559730	NM_003287.4(TPD52L1):c.604C>G (p.Leu202Val)	TPD52L1 (L173V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar