ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.55664C>T (p.Ala18555Val)

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 RCV002435300 SCV002748510 uncertain significance Cardiovascular phenotype 2019-11-08 criteria provided, single submitter clinical testing The p.A9490V variant (also known as c.28469C>T), located in coding exon 114 of the TTN gene, results from a C to T substitution at nucleotide position 28469. The alanine at codon 9490 is replaced by valine, an amino acid with similar properties. This amino acid position is highly conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. 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.