List of variants in gene CUBN reported by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001081.4(CUBN):c.3088C>A (p.Leu1030Ile)	rs746111876	0.00003
NM_001081.4(CUBN):c.10233G>A (p.Trp3411Ter)	rs144484373	0.00002
NM_001081.4(CUBN):c.5318G>A (p.Gly1773Asp)	rs776483762	0.00001
NM_001081.4(CUBN):c.6894_6901dup (p.Leu2301Ter)	rs1399856074	0.00001
NM_001081.4(CUBN):c.10009_10012del (p.Leu3337fs)	rs2491157416
NM_001081.4(CUBN):c.2839G>T (p.Gly947Cys)	rs2131844929
NM_001081.4(CUBN):c.3889C>T (p.Pro1297Ser)	rs2491931442
NM_001081.4(CUBN):c.4350+5G>A	rs200324164
NM_001081.4(CUBN):c.5913_5916del (p.Thr1972fs)	rs765301342
NM_001081.4(CUBN):c.9273C>G (p.Cys3091Trp)	rs558940054

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.