List of variants in gene DGUOK reported as benign for not provided

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: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_000002.12:g.73926778C>T	rs831526	0.98942
NM_080916.3(DGUOK):c.591+221T>C	rs7564379	0.69496
NM_080916.3(DGUOK):c.443+112A>G	rs940297	0.68875
NM_080916.3(DGUOK):c.143-181G>A	rs831527	0.55665
NM_080916.3(DGUOK):c.707+206G>A	rs2002711	0.45303
NM_080916.3(DGUOK):c.707+310T>C	rs4077241	0.09444
NM_080916.3(DGUOK):c.255+277T>A	rs59485700	0.07477
NM_080916.3(DGUOK):c.444-353A>G	rs79216512	0.05978
NM_080916.3(DGUOK):c.444-170G>A	rs11884185	0.05655
NM_080916.3(DGUOK):c.159G>A (p.Thr53=)	rs62641680	0.01745
NM_080916.3(DGUOK):c.423G>A (p.Glu141=)	rs1804599	0.01535
NM_080916.3(DGUOK):c.509A>G (p.Gln170Arg)	rs74874677	0.01472
NC_000002.12:g.73926524del	rs35826941
NC_000002.12:g.73926872_73926886del	rs759288670
NM_080916.3(DGUOK):c.206_210dup	rs554820333
NM_080916.3(DGUOK):c.256-14del	rs1259926103
NM_080916.3(DGUOK):c.256-190A>C	rs1523828

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.