List of variants in gene CUBN reported as pathogenic for Proteinuria, chronic benign

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.4689T>A (p.Cys1563Ter)	rs558840029	0.00009
NM_001081.4(CUBN):c.10009_10012del (p.Leu3337fs)	rs2491157416
NM_001081.4(CUBN):c.4689_4690delinsAT (p.Cys1563_Ile1564delinsTer)	rs2131697094
NM_001081.4(CUBN):c.4753C>T (p.Gln1585Ter)
NM_001081.4(CUBN):c.4774_4775del (p.Ser1592fs)
NM_001081.4(CUBN):c.5913_5916del (p.Thr1972fs)	rs765301342

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