List of variants in gene KNL1 reported as likely benign for not specified

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: 18

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_144508.5(KNL1):c.4339A>G (p.Thr1447Ala)	rs16970911	0.06529
NM_144508.5(KNL1):c.245T>C (p.Met82Thr)	rs79413475	0.03753
NM_144508.5(KNL1):c.2369C>G (p.Thr790Ser)	rs33931006	0.01841
NM_144508.5(KNL1):c.1493T>A (p.Ile498Asn)	rs59648663	0.01046
NM_144508.5(KNL1):c.5151T>C (p.Pro1717=)	rs74377704	0.00815
NM_144508.5(KNL1):c.2014A>C (p.Ile672Leu)	rs73394756	0.00510
NM_144508.5(KNL1):c.6034A>G (p.Ile2012Val)	rs74970544	0.00405
NM_144508.5(KNL1):c.1299T>C (p.Cys433=)	rs35235972	0.00349
NM_144508.5(KNL1):c.1129A>G (p.Ile377Val)	rs144726295	0.00317
NM_144508.5(KNL1):c.1233G>C (p.Met411Ile)	rs116093409	0.00245
NM_144508.5(KNL1):c.*7G>C	rs565293268	0.00144
NM_144508.5(KNL1):c.*8G>T	rs758759341	0.00144
NM_144508.5(KNL1):c.4_5insAT	rs538937570	0.00143
NM_144508.5(KNL1):c.165C>T (p.Asn55=)	rs201818761	0.00125
NM_144508.5(KNL1):c.3999C>T (p.Cys1333=)	rs373793762	0.00098
NM_144508.5(KNL1):c.5631C>T (p.Leu1877=)	rs201853975	0.00066
NM_144508.5(KNL1):c.4903C>T (p.Leu1635=)	rs1216173133
NM_170589.4(KNL1):c.2_3ins13

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.