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Renal Hereditary Cancer Panel, Sequencing and Deletion/Duplication, 15 Genes

CPT Code(s): 81292; 81294; 81295; 81297; 81298; 81300; 81321; 81323; 81403 (VHL); 81404 x3 (SDHC, SDHD, VHL); 81405 x5 (FH, SDHB, SDHC, TP53, TSC1); 81406 x2 (TSC1, TSC2); 81407 (TSC2); 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:Refrigerated.
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/Duplication2007167 Hereditary Paraganglioma-Pheochromocytoma (SDHB, SDHC, and SDHD) Sequencing and Deletion/Dup2009313 Li-Fraumeni (TP53) Sequencing and Deletion/DuplicationBAP1, FH, FLCN, MET, MLH1, MSH2, MSH6, PTEN, SDHB, SDHC, SDHD, TP53, TSC1, TSC2, VHLBirt-Hogg-Dube syndromeCowden syndromeTuberous sclerosis (TS)
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