"AiLife Diagnostics, AiLife Diagnostics"[submitter] AND "CUBN"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 522507	NM_001081.4(CUBN):c.9053A>C (p.Tyr3018Ser)	CUBN (Y3018S)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1678498	NM_001081.4(CUBN):c.8284C>A (p.Gln2762Lys)	CUBN (Q2762K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1678499	NM_001081.4(CUBN):c.7003C>T (p.Gln2335Ter)	CUBN (Q2335*)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic

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