"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "MEPE"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 767958	NM_020203.6(MEPE):c.1171G>A (p.Ala391Thr)	MEPE (A278T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 767959	NM_020203.6(MEPE):c.1185C>G (p.Asn395Lys)	MEPE (N395K +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 767960	NM_020203.6(MEPE):c.1240T>G (p.Ser414Ala)	MEPE (S301A +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 767961	NM_020203.6(MEPE):c.1346A>C (p.Asn449Thr)	MEPE (N449T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 767962	NM_020203.6(MEPE):c.1441C>T (p.Arg481Trp)	MEPE (R481W +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 767963	NM_020203.6(MEPE):c.1461A>C (p.Gln487His)	MEPE (Q487H +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3246698	NC_000004.11:g.(?_88532061)_(89190078_?)dup	ABCG2, DMP1 +6 more	Duplication	Autosomal dominant polycystic kidney disease	GUncertain significance

ClinVar