List of variants in gene CUBN reported as likely pathogenic by Revvity Omics, Revvity

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.348+2T>C	rs146047781	0.00012
NM_001081.4(CUBN):c.10311dup (p.His3438fs)	rs1200249069
NM_001081.4(CUBN):c.2496dup (p.Pro833fs)	rs1554816715

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