ClinVar Miner

Submissions for variant NM_013275.6(ANKRD11):c.6985G>C (p.Val2329Leu) (rs760933701)

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 RCV000719005 SCV000849869 uncertain significance Autism spectrum disorder 2017-05-31 criteria provided, single submitter clinical testing The p.V2329L variant (also known as c.6985G>C), located in coding exon 7 of the ANKRD11 gene, results from a G to C substitution at nucleotide position 6985. The valine at codon 2329 is replaced by leucine, an amino acid with highly similar properties. This amino acid position is not 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.