Total submissions: 10
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000164506 | SCV000215157 | likely benign | Hereditary cancer-predisposing syndrome | 2019-09-11 | criteria provided, single submitter | clinical testing | Synonymous alterations with insufficient evidence to classify as benign |
Invitae | RCV000198476 | SCV000253637 | likely benign | Fanconi anemia, complementation group O | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Counsyl | RCV000198476 | SCV000490087 | likely benign | Fanconi anemia, complementation group O | 2016-11-02 | criteria provided, single submitter | clinical testing | |
Counsyl | RCV000410680 | SCV000490088 | likely benign | Breast-ovarian cancer, familial 3 | 2016-11-02 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000445007 | SCV000521532 | likely benign | not specified | 2017-07-27 | 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. |
Quest Diagnostics Nichols Institute San Juan Capistrano | RCV000445007 | SCV000602134 | likely benign | not specified | 2017-03-02 | criteria provided, single submitter | clinical testing | |
Color | RCV000164506 | SCV000686325 | likely benign | Hereditary cancer-predisposing syndrome | 2015-08-11 | criteria provided, single submitter | clinical testing | |
Quest Diagnostics Nichols Institute San Juan Capistrano | RCV000760057 | SCV000889816 | likely benign | not provided | 2018-03-07 | criteria provided, single submitter | clinical testing | |
Mendelics | RCV000198476 | SCV001140707 | likely benign | Fanconi anemia, complementation group O | 2019-05-28 | criteria provided, single submitter | clinical testing | |
Integrated Genetics/Laboratory Corporation of America | RCV000445007 | SCV001362535 | likely benign | not specified | 2019-08-27 | criteria provided, single submitter | clinical testing |