ClinVar Miner

Submissions for variant NM_000246.4(CIITA):c.673G>A (p.Gly225Arg)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV003337965 SCV004048436 uncertain significance Rheumatoid arthritis criteria provided, single submitter clinical testing The missense variant in c.676G>A (p.Gly226Arg) in CIITA gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Gly226Arg variant is novel (not in any individuals) in gnomAD Exomes and 1000 Genomes. The amino acid Gly at position 226 is changed to a Arg changing protein sequence and it might alter its composition and physico-chemical properties. The variant is predicted to be damaging by both SIFT and PolyPhen2. The residue is conserved across species. The amino acid change p.Gly226Arg in CIITA is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. For these reasons, this variant has been classified as Uncertain Significance.

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.