Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Ambry Genetics | RCV000571822 | SCV000671906 | uncertain significance | Hereditary cancer-predisposing syndrome | 2017-01-06 | criteria provided, single submitter | clinical testing | The p.F164V variant (also known as c.490T>G), located in coding exon 3 of the RAD51C gene, results from a T to G substitution at nucleotide position 490. The phenylalanine at codon 164 is replaced by valine, an amino acid with highly similar 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. |
| Labcorp Genetics |
RCV003617834 | SCV004454663 | uncertain significance | Fanconi anemia complementation group O | 2023-04-15 | criteria provided, single submitter | clinical testing | ClinVar contains an entry for this variant (Variation ID: 484746). 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 expected to disrupt RAD51C protein function. This variant has not been reported in the literature in individuals affected with RAD51C-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces phenylalanine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 164 of the RAD51C protein (p.Phe164Val). |