List of variants reported as likely pathogenic for Syndromic X-linked intellectual disability 14

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_080632.3(UPF3B):c.846+1G>A	rs373920032	0.00001
NM_080632.3(UPF3B):c.1060C>T (p.Arg354Ter)	rs2056119926
NM_080632.3(UPF3B):c.1147G>T (p.Glu383Ter)	rs1480554912
NM_080632.3(UPF3B):c.240del (p.Phe80fs)	rs2521576667
NM_080632.3(UPF3B):c.270T>G (p.Tyr90Ter)	rs2521574129
NM_080632.3(UPF3B):c.646_647del (p.Glu216fs)	rs2521526324
NM_080632.3(UPF3B):c.982G>T (p.Glu328Ter)	rs376175156

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.