Total submissions: 5
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Ambry Genetics | RCV000216447 | SCV000277274 | likely benign | Hereditary cancer-predisposing syndrome | 2017-11-29 | criteria provided, single submitter | clinical testing | This alteration is classified as likely benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. |
| Gene |
RCV001705224 | SCV000730240 | likely benign | not provided | 2020-08-21 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 27997549) |
| Invitae | RCV000689233 | SCV000816874 | uncertain significance | Familial cancer of breast | 2023-11-27 | criteria provided, single submitter | clinical testing | This sequence change replaces glycine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 203 of the BARD1 protein (p.Gly203Arg). This variant is present in population databases (no rsID available, gnomAD no frequency). This variant has not been reported in the literature in individuals affected with BARD1-related conditions. ClinVar contains an entry for this variant (Variation ID: 232988). Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Not Available"; PolyPhen-2: "Benign"; Align-GVGD: "Not Available". The arginine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect 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. |
| Color Diagnostics, |
RCV000216447 | SCV000905504 | likely benign | Hereditary cancer-predisposing syndrome | 2017-10-27 | criteria provided, single submitter | clinical testing | |
| KCCC/NGS Laboratory, |
RCV000689233 | SCV004016364 | likely benign | Familial cancer of breast | 2023-07-07 | criteria provided, single submitter | clinical testing |