"Baylor Genetics"[submitter] AND "CUBN"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 299396	NM_001081.4(CUBN):c.8701G>A (p.Val2901Ile)	CUBN (V2901I)	Single nucleotide variant (missense variant)	CUBN-related disorder +3 more	GUncertain significance
Select item 878998	NM_001081.4(CUBN):c.7837A>C (p.Ile2613Leu)	CUBN (I2613L)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1033272	NM_001081.4(CUBN):c.7406C>T (p.Pro2469Leu)	CUBN (P2469L)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1 +1 more	GUncertain significance
Select item 299463	NM_001081.4(CUBN):c.5305G>C (p.Val1769Leu)	CUBN (V1769L)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1 +2 more	GUncertain significance
Select item 546272	NM_001081.4(CUBN):c.4669C>T (p.Leu1557Phe)	CUBN (L1557F)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1 +2 more	GConflicting classifications of pathogenicity
Select item 1029049	NM_001081.4(CUBN):c.265A>C (p.Lys89Gln)	CUBN (K89Q)	Single nucleotide variant (missense variant)	Imerslund-Grasbeck syndrome type 1 +1 more	GUncertain significance

ClinVar