List of variants in gene IFT74 reported as likely pathogenic for ciliopathy

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_025103.4(IFT74):c.120+2dup	rs551515830	0.00048
NM_025103.4(IFT74):c.1685-1G>T	rs200699377	0.00005
NM_025103.4(IFT74):c.535C>G (p.Gln179Glu)	rs150219690	0.00004
NM_025103.4(IFT74):c.1054G>T (p.Gly352Cys)	rs759662469	0.00001
NM_025103.4(IFT74):c.85C>T (p.Arg29Ter)	rs751583919	0.00001
GRCh38/hg38 9p21.2(chr9:27040565-27060992)
NM_025103.4(IFT74):c.-19-2025_120+884delinsTTA
NM_025103.4(IFT74):c.358G>T (p.Glu120Ter)
NM_025103.4(IFT74):c.853G>T (p.Glu285Ter)	rs1056125920

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.