ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.90656T>G (p.Val30219Gly)

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 RCV002368944 SCV002659529 uncertain significance Cardiovascular phenotype 2018-05-02 criteria provided, single submitter clinical testing The p.V21154G variant (also known as c.63461T>G), located in coding exon 162 of the TTN gene, results from a T to G substitution at nucleotide position 63461. The valine at codon 21154 is replaced by glycine, an amino acid with dissimilar properties. This amino acid position is poorly 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.