List of variants in gene combination IFT80, TRIM59-IFT80 reported as uncertain significance by Eurofins Ntd Llc (ga)

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020800.3(IFT80):c.60G>A (p.Val20=)	rs201088893	0.00050
NM_020800.3(IFT80):c.721G>C (p.Gly241Arg)	rs138004478	0.00043
NM_020800.3(IFT80):c.1883G>A (p.Arg628Gln)	rs150370681	0.00038
NM_020800.3(IFT80):c.2158C>A (p.Gln720Lys)	rs201820395	0.00021
NM_020800.3(IFT80):c.2307C>T (p.Ser769=)	rs565364572	0.00005
NM_020800.3(IFT80):c.1825C>T (p.Arg609Cys)	rs186192085	0.00003
NM_020800.3(IFT80):c.1150A>C (p.Arg384=)	rs1559928711
NM_020800.3(IFT80):c.1468A>G (p.Ile490Val)	rs1559917807
NM_020800.3(IFT80):c.1769C>T (p.Ala590Val)	rs766857775
NM_020800.3(IFT80):c.1837-6_1837-2del	rs780412409

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.