Total submissions: 4
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Ambry Genetics | RCV000220255 | SCV000277298 | uncertain significance | Hereditary cancer-predisposing syndrome | 2023-02-19 | criteria provided, single submitter | clinical testing | The p.S204A variant (also known as c.610T>G), located in coding exon 5 of the BRIP1 gene, results from a T to G substitution at nucleotide position 610. The serine at codon 204 is replaced by alanine, an amino acid with similar properties. This amino acid position is 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. |
| Labcorp Genetics |
RCV000636121 | SCV000757553 | uncertain significance | Familial cancer of breast; Fanconi anemia complementation group J | 2023-03-20 | criteria provided, single submitter | clinical testing | 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 BRIP1 protein function. ClinVar contains an entry for this variant (Variation ID: 233008). This variant has not been reported in the literature in individuals affected with BRIP1-related conditions. This variant is present in population databases (rs761401027, gnomAD 0.0009%). This sequence change replaces serine, which is neutral and polar, with alanine, which is neutral and non-polar, at codon 204 of the BRIP1 protein (p.Ser204Ala). |
| Gene |
RCV002307457 | SCV002601450 | uncertain significance | not provided | 2022-05-12 | criteria provided, single submitter | clinical testing | Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge |
| Baylor Genetics | RCV004567628 | SCV005059921 | uncertain significance | Familial cancer of breast | 2023-12-23 | criteria provided, single submitter | clinical testing |