Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000438715 | SCV000526936 | likely benign | not specified | 2017-08-02 | criteria provided, single submitter | clinical testing | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. |
Invitae | RCV000539994 | SCV000633176 | likely benign | Familial cancer of breast | 2023-12-14 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000575675 | SCV000675998 | likely benign | Hereditary cancer-predisposing syndrome | 2016-09-07 | 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. |
Color Diagnostics, |
RCV000575675 | SCV002052648 | likely benign | Hereditary cancer-predisposing syndrome | 2021-04-13 | criteria provided, single submitter | clinical testing |