Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001502366 | SCV001707199 | likely benign | BAP1-related tumor predisposition syndrome | 2019-10-19 | criteria provided, single submitter | clinical testing | |
Myriad Genetics, |
RCV001502366 | SCV005403495 | benign | BAP1-related tumor predisposition syndrome | 2024-07-16 | criteria provided, single submitter | clinical testing | This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing. |