Specimen Collection Manual and Test Catalog
LI-FRAUMENI SYNDROME, TP53 SEQUENCING AND DELETION/DUPLICATION
Geisinger Epic Procedure Code: LAB1336 Geisinger Epic ID: 53269Whole blood
5 mL whole blood; minimum 2 mL.
Send report of results for family member with known BRCA mutation.
Specimen stability is crucial. Store and ship room temperature immediately. Do not freeze.
Room temperature: 14 days. Refrigerated: 14 days. Frozen: Unacceptable.
Gross hemolysis • Clotted specimens
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
The CPT codes provided by GML are based on AMA guidelines and are for informational purposes only.
Long-Range Polymerase Chain Reaction
Next Generation Sequencing with Microarray Confirmation
Quest test code 92560, Li-Fraumeni
Mutations in the TP53 gene leads to Li-Fraumeni syndrome (LFS) which is an inherited cancer syndrome with an early onset of tumors, multiple tumors within an individual, and often multiple affected family members. The most common types of tumors are soft tissue sarcomas and osteosarcomas, breast cancer, brain tumors, leukemia, and adrenocortical carcinoma. Sequencing and deletion/duplication analyses of the TP53 gene will identify individuals who are affected with LFS and therefore at risk for TP53-related cancers.