Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000465409 | SCV000544556 | benign | Tuberous sclerosis 2 | 2023-05-30 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV002451089 | SCV002614271 | uncertain significance | Hereditary cancer-predisposing syndrome | 2021-11-04 | criteria provided, single submitter | clinical testing | The p.G1123E variant (also known as c.3368G>A), located in coding exon 28 of the TSC2 gene, results from a G to A substitution at nucleotide position 3368. The glycine at codon 1123 is replaced by glutamic acid, an amino acid with similar properties. This amino acid position is not 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. |