ClinVar Miner

Submissions for variant NM_013275.6(ANKRD11):c.7799G>A (p.Arg2600His) (rs1354874973)

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
Ambry Genetics RCV000720019 SCV000850893 uncertain significance Autism spectrum disorder 2017-05-24 criteria provided, single submitter clinical testing The p.R2600H variant (also known as c.7799G>A), located in coding exon 10 of the ANKRD11 gene, results from a G to A substitution at nucleotide position 7799. The arginine at codon 2600 is replaced by histidine, an amino acid with highly similar properties. This amino acid position is well conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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.