List of variants in gene NBN reported as likely benign for 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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002485.5(NBN):c.37+5G>A	rs116735828	0.00767
NM_002485.5(NBN):c.1720T>A (p.Leu574Ile)	rs142334798	0.00044
NM_002485.5(NBN):c.1690G>A (p.Glu564Lys)	rs72550742	0.00030
NM_002485.5(NBN):c.1262T>C (p.Leu421Ser)	rs104895032	0.00027
NM_002485.5(NBN):c.2220T>C (p.Ala740=)	rs147494981	0.00019
NM_002485.5(NBN):c.1809C>A (p.Phe603Leu)	rs192236678	0.00014
NM_002485.5(NBN):c.1124+6G>T	rs375862750	0.00013
NM_002485.5(NBN):c.1036G>A (p.Val346Met)	rs200297914	0.00011
NM_002485.5(NBN):c.37+10G>C	rs369408590	0.00011
NM_002485.5(NBN):c.819A>T (p.Thr273=)	rs147660518	0.00006
NM_002485.5(NBN):c.930T>A (p.Ile310=)	rs142813526	0.00006
NM_002485.5(NBN):c.896+13T>G	rs376695206	0.00003
NM_002485.5(NBN):c.306T>C (p.Phe102=)	rs1554568276	0.00001
NM_002485.5(NBN):c.1124+11_1124+13del	rs747584990
NM_002485.5(NBN):c.2082T>C (p.Pro694=)	rs7823648
NM_002485.5(NBN):c.481-11C>T	rs2129890419

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.