Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV002310943 | SCV000319585 | uncertain significance | Familial thoracic aortic aneurysm and aortic dissection | 2021-06-30 | criteria provided, single submitter | clinical testing | The p.G690R variant (also known as c.2068G>A), located in coding exon 13 of the NOTCH1 gene, results from a G to A substitution at nucleotide position 2068. The glycine at codon 690 is replaced by arginine, an amino acid with dissimilar properties. This amino acid position is highly conserved in available vertebrate species. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear. |
Blueprint Genetics | RCV000788401 | SCV000927495 | uncertain significance | not provided | 2017-12-13 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV002270160 | SCV002553912 | uncertain significance | Adams-Oliver syndrome 5 | 2022-03-15 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV002270159 | SCV002553913 | uncertain significance | Aortic valve disease 1 | 2022-03-15 | criteria provided, single submitter | clinical testing |