List of variants in gene CUBN reported as pathogenic by GeneDx

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.7906C>T (p.Arg2636Ter)	rs137998687	0.00015
NM_001081.4(CUBN):c.6088C>T (p.Arg2030Ter)	rs374417889	0.00003
NM_001081.4(CUBN):c.6359G>A (p.Trp2120Ter)	rs566060177	0.00003
NM_001081.4(CUBN):c.1865del (p.Thr622fs)	rs386833771	0.00001
NM_001081.4(CUBN):c.6821+3A>G	rs767078847	0.00001
NM_001081.4(CUBN):c.6928_6934del (p.Glu2310fs)	rs757649673

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