Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV002315142 | SCV000739514 | uncertain significance | Familial thoracic aortic aneurysm and aortic dissection | 2023-03-31 | criteria provided, single submitter | clinical testing | The p.N918S variant (also known as c.2753A>G), located in coding exon 18 of the NOTCH1 gene, results from an A to G substitution at nucleotide position 2753. The asparagine at codon 918 is replaced by serine, an amino acid with highly 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. |
Invitae | RCV000655233 | SCV000777163 | benign | Adams-Oliver syndrome 5 | 2023-10-16 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV000655233 | SCV002553530 | uncertain significance | Adams-Oliver syndrome 5 | 2022-03-15 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV002270923 | SCV002553531 | uncertain significance | Aortic valve disease 1 | 2022-03-15 | criteria provided, single submitter | clinical testing |