List of variants in gene KIF14 reported as uncertain significance for autosomal recessive disease

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014875.3(KIF14):c.1184C>T (p.Thr395Met)	rs138621008	0.00238
NM_014875.3(KIF14):c.4843G>A (p.Gly1615Ser)	rs146186348	0.00026
NM_014875.3(KIF14):c.1009G>A (p.Glu337Lys)	rs147387069	0.00011
NM_014875.3(KIF14):c.1375G>A (p.Gly459Arg)	rs1660302910	0.00001
NM_014875.3(KIF14):c.595A>G (p.Thr199Ala)	rs765579360	0.00001
NM_014875.3(KIF14):c.1570C>G (p.His524Asp)	rs1659904063
NM_014875.3(KIF14):c.1979+2C>T
NM_014875.3(KIF14):c.3127C>T (p.His1043Tyr)	rs763872222
NM_014875.3(KIF14):c.3136C>T (p.Arg1046Cys)
NM_014875.3(KIF14):c.4247C>A (p.Ala1416Asp)	rs372382009
NM_014875.3(KIF14):c.4353+7T>A

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.