List of variants in gene UNC13D reported as benign by PreventionGenetics, part of Exact Sciences

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: 28

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.3198A>G (p.Glu1066=)	rs7210574	0.49757
NM_199242.3(UNC13D):c.2599A>G (p.Lys867Glu)	rs1135688	0.47045
NM_199242.3(UNC13D):c.154-19G>A	rs3744009	0.24392
NM_199242.3(UNC13D):c.1596+36A>G	rs3744026	0.23763
NM_199242.3(UNC13D):c.1728-48T>C	rs3744024	0.23380
NM_199242.3(UNC13D):c.1992+5G>A	rs17581728	0.19407
NM_199242.3(UNC13D):c.2299-46C>T	rs7212635	0.18407
NM_199242.3(UNC13D):c.117+30G>A	rs3744011	0.10282
NM_199242.3(UNC13D):c.754-31C>T	rs7226310	0.09910
NM_199242.3(UNC13D):c.1389+36G>A	rs74410877	0.08586
NM_199242.3(UNC13D):c.1390-38T>C	rs112501005	0.02851
NM_199242.3(UNC13D):c.1744C>T (p.Leu582=)	rs75853379	0.02622
NM_199242.3(UNC13D):c.1977C>T (p.Thr659=)	rs2290770	0.02469
NM_199242.3(UNC13D):c.262-17G>A	rs142996967	0.01903
NM_199242.3(UNC13D):c.1579C>T (p.Arg527Trp)	rs75366116	0.01644
NM_199242.3(UNC13D):c.951+13T>G	rs140758914	0.01637
NM_199242.3(UNC13D):c.175G>A (p.Ala59Thr)	rs9904366	0.01403
NM_199242.3(UNC13D):c.3252T>C (p.His1084=)	rs61753922	0.01313
NM_199242.3(UNC13D):c.1992+11T>C	rs112501965	0.01262
NM_199242.3(UNC13D):c.904C>T (p.Leu302Phe)	rs55661958	0.01066
NM_199242.3(UNC13D):c.2298+15C>T	rs112341334	0.00741
NM_199242.3(UNC13D):c.847A>G (p.Ile283Val)	rs61754871	0.00194
NM_199242.3(UNC13D):c.24G>A (p.Pro8=)	rs143320460	0.00095
NM_199242.3(UNC13D):c.99G>A (p.Pro33=)	rs147886860	0.00090
NM_199242.3(UNC13D):c.2448-8dup	rs3217698
NM_199242.3(UNC13D):c.261+26C>G	rs3744008
NM_199242.3(UNC13D):c.279C>T (p.Pro93=)	rs3744007
NM_199242.3(UNC13D):c.888G>C (p.Pro296=)	rs7223416

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.