Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Labcorp Genetics |
RCV002013897 | SCV002299416 | uncertain significance | Peutz-Jeghers syndrome | 2022-03-03 | criteria provided, single submitter | clinical testing | 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 expected to disrupt STK11 protein function. 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. This variant has not been reported in the literature in individuals affected with STK11-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces threonine, which is neutral and polar, with methionine, which is neutral and non-polar, at codon 71 of the STK11 protein (p.Thr71Met). |
| Ambry Genetics | RCV002423247 | SCV002729983 | uncertain significance | Hereditary cancer-predisposing syndrome | 2020-01-24 | criteria provided, single submitter | clinical testing | The p.T71M variant (also known as c.212C>T), located in coding exon 1 of the STK11 gene, results from a C to T substitution at nucleotide position 212. The threonine at codon 71 is replaced by methionine, an amino acid with 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. |