Total submissions: 4
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Invitae | RCV003537067 | SCV000647444 | uncertain significance | Familial adenomatous polyposis 1 | 2023-08-22 | 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 APC protein function. ClinVar contains an entry for this variant (Variation ID: 469919). This variant has not been reported in the literature in individuals affected with APC-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.01%). This sequence change replaces histidine, which is basic and polar, with aspartic acid, which is acidic and polar, at codon 1119 of the APC protein (p.His1119Asp). |
| Ambry Genetics | RCV001020068 | SCV001181499 | uncertain significance | Hereditary cancer-predisposing syndrome | 2020-08-24 | criteria provided, single submitter | clinical testing | The p.H1119D variant (also known as c.3355C>G), located in coding exon 15 of the APC gene, results from a C to G substitution at nucleotide position 3355. The histidine at codon 1119 is replaced by aspartic acid, 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. |
| Quest Diagnostics Nichols Institute San Juan Capistrano | RCV001284356 | SCV001470101 | uncertain significance | not provided | 2020-08-14 | criteria provided, single submitter | clinical testing | |
| Gene |
RCV001284356 | SCV004034753 | uncertain significance | not provided | 2023-03-07 | 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; This variant is associated with the following publications: (PMID: 18199528, 30709382) |