ClinVar Miner

List of variants in gene CUBN reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
NM_001081.3(CUBN):c.1349G>A (p.Gly450Asp) rs146463364
NM_001081.3(CUBN):c.2756A>G (p.His919Arg) rs148869805
NM_001081.3(CUBN):c.4268C>T (p.Thr1423Met) rs483352704
NM_001081.3(CUBN):c.5069C>T (p.Ala1690Val) rs141640975
NM_001081.3(CUBN):c.5081-106_5081-105insTAGTGGCAAA rs778548191
NM_001081.3(CUBN):c.5840C>A (p.Ser1947Tyr) rs147617753
NM_001081.3(CUBN):c.6268A>G (p.Lys2090Glu) rs201374966
NM_001081.3(CUBN):c.6479A>G (p.Asp2160Gly) rs144704318
NM_001081.3(CUBN):c.6613G>A (p.Gly2205Arg) rs140883483
NM_001081.3(CUBN):c.7400A>G (p.Asn2467Ser) rs200197243
NM_001081.3(CUBN):c.8720C>A (p.Ala2907Glu) rs758557930
NM_001081.3(CUBN):c.8894T>C (p.Phe2965Ser) rs117620008

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.