Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV002313395 | SCV000739170 | uncertain significance | Familial thoracic aortic aneurysm and aortic dissection | 2017-12-14 | criteria provided, single submitter | clinical testing | The p.V1927I variant (also known as c.5779G>A), located in coding exon 40 of the MED12 gene, results from a G to A substitution at nucleotide position 5779. The valine at codon 1927 is replaced by isoleucine, 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. |