List of variants in gene CBL reported as benign for immune system cancer

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_005188.4(CBL):c.1095+19G>T	rs2510152	0.61865
NM_005188.4(CBL):c.2592C>T (p.Leu864=)	rs1893177	0.03391
NM_005188.4(CBL):c.869+4A>G	rs77284821	0.02038
NM_005188.4(CBL):c.513T>C (p.Ser171=)	rs2227987	0.00741
NM_005188.4(CBL):c.1485G>A (p.Pro495=)	rs2229072	0.00547
NM_005188.4(CBL):c.2710G>A (p.Val904Ile)	rs17122769	0.00454
NM_005188.4(CBL):c.869+19A>G	rs181589369	0.00232
NM_005188.4(CBL):c.1359A>C (p.Pro453=)	rs34732429	0.00188
NM_005188.4(CBL):c.2484G>A (p.Pro828=)	rs149533467	0.00166
NM_005188.4(CBL):c.2190G>C (p.Thr730=)	rs143840974	0.00137
NM_005188.4(CBL):c.1858C>T (p.Leu620Phe)	rs2227988	0.00121
NM_005188.4(CBL):c.2269G>A (p.Ala757Thr)	rs146517083	0.00076
NM_005188.4(CBL):c.1641T>C (p.Pro547=)	rs61755280	0.00074
NM_005188.4(CBL):c.1227+4C>T	rs201747825	0.00048
NM_005188.4(CBL):c.1629A>G (p.Pro543=)	rs558577411

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.