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Central Nervous System Hereditary Cancer Panel, Sequencing and Deletion/Duplication, 15 Genes

CPT Code(s): 81201 (APC); 81203 (APC); 81292 (MLH1); 81294 (MLH1); 81295 (MSH2); 81297 (MSH2); 81298 (MSH6); 81300 (MSH6); 81321 (PTEN); 81323 (PTEN); 81403 x2 (PHOX2B, VHL); 81404 x3 (PHOX2B, STK11, VHL); 81405 x3 (NF2, STK11, TP53); 81406 (NF2); 81479 x2
Specimen Required: Patient Preparation:
Collect:Lavender (EDTA) or yellow (ACD Solution A or B).
Specimen Preparation:Transport 3 mL whole blood. (Min: 1 mL)
Storage/Transport Temperature:
Stability:Ambient: 72 hours; Refrigerated: 1 week; Frozen: Unacceptable
New York DOH Approval Status: Specimens from New York clients will be sent out to a New York DOH approved laboratory, if possible.
Aliases:
  • 0051650 HNPCC/Lynch Syndrome (MLH1) Sequencing and Deletion/Duplication0051654 HNPCC/Lynch Syndrome (MSH2) Sequencing and Deletion/Duplication0051656 HNPCC/Lynch Syndrome (MSH6) Sequencing and Deletion/Duplication2002470 PTEN-Related Disorders (PTEN) Sequencing and Deletion/Duplication2002965 von Hippel-Lindau (VHL) Sequencing and Deletion/Duplication2004863 Familial Adenomatous Polyposis (APC) Sequencing2008398 Peutz-Jeghers Syndrome (STK11) Sequencing and Deletion/Duplication2009313 Li-Fraumeni (TP53) Sequencing and Deletion/DuplicationALK, APC, BAP1, MLH1, MSH2, MSH6, NF2, PHOX2B, PTEN, RB1, SMARCB1, STK11, SUFU, TP53, VHLCNS tumorCowden syndrome
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