Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001913683 | SCV002184073 | benign | Adams-Oliver syndrome 5 | 2022-11-01 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002361222 | SCV002663204 | uncertain significance | Familial thoracic aortic aneurysm and aortic dissection | 2019-03-28 | criteria provided, single submitter | clinical testing | The p.V2213M variant (also known as c.6637G>A), located in coding exon 34 of the NOTCH1 gene, results from a G to A substitution at nucleotide position 6637. The valine at codon 2213 is replaced by methionine, an amino acid with highly similar properties. This amino acid position is well 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. |