Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Labcorp Genetics |
RCV001206026 | SCV001377313 | uncertain significance | Neurofibromatosis, type 1 | 2022-11-15 | criteria provided, single submitter | clinical testing | This sequence change replaces threonine, which is neutral and polar, with serine, which is neutral and polar, at codon 1544 of the NF1 protein (p.Thr1544Ser). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt NF1 protein function. ClinVar contains an entry for this variant (Variation ID: 937080). This variant has not been reported in the literature in individuals affected with NF1-related conditions. This variant is not present in population databases (gnomAD no frequency). |
| Ambry Genetics | RCV002339522 | SCV002635240 | uncertain significance | Hereditary cancer-predisposing syndrome; Cardiovascular phenotype | 2019-06-20 | criteria provided, single submitter | clinical testing | The p.T1544S variant (also known as c.4631C>G), located in coding exon 34 of the NF1 gene, results from a C to G substitution at nucleotide position 4631. The threonine at codon 1544 is replaced by serine, an amino acid with similar properties. This amino acid position is highly 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. |