List of variants in gene CUBN reported as pathogenic by MVZ Medizinische Genetik Mainz

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.4042G>T (p.Gly1348Ter)	rs2491869860
NM_001081.4(CUBN):c.4753C>T (p.Gln1585Ter)
NM_001081.4(CUBN):c.4774_4775del (p.Ser1592fs)
NM_001081.4(CUBN):c.6297_6298insT (p.Arg2100Ter)	rs2491477929
NM_001081.4(CUBN):c.9286_9287del (p.Leu3096fs)

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