"Ambry Genetics"[submitter] AND "LIN52"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3118929	NM_001024674.3(LIN52):c.64C>T (p.Arg22Cys)	LIN52 (R20C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336410	NM_001024674.3(LIN52):c.107C>T (p.Ala36Val)	LIN52 (A36V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290767	NM_001024674.3(LIN52):c.126C>G (p.Phe42Leu)	LIN52 (F40L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233162	NM_001024674.3(LIN52):c.152C>G (p.Pro51Arg)	LIN52 (P51R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602579	NM_001024674.3(LIN52):c.176G>A (p.Arg59His)	LIN52 (R59H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283819	NM_001024674.3(LIN52):c.187G>A (p.Asp63Asn)	LIN52 (D61N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118927	NM_001024674.3(LIN52):c.218C>T (p.Thr73Met)	LIN52 (T71M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar