EPOR Mutation Detection by Sequencing
2007914
 
Ordering Recommendation
Preferred test for confirming Primary Familial or Congenital Polycythemia (PFCP).
Mnemonic
EPOR
Methodology
Polymerase Chain Reaction/Sequencing
Performed
DNA Isolation: Sun-Sat
Assay: Varies
Reported
12-14 days
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
 
Collect
Lavender (EDTA).  
Specimen Preparation
Transport 5 mL whole blood. (Min: 1 mL)  
Storage/Transport Temperature
Refrigerated.  
Unacceptable Conditions
Serum or plasma. Specimens collected in anticoagulants other than EDTA. Clotted or severely hemolyzed specimens.  
Remarks
 
Stability
Ambient: 24 hours; Refrigerated: 5 days; Frozen: Unacceptable  
Reference Interval
Interpretive Data
Refer to report.

See Compliance Statement B: www.aruplab.com/CS
Note
CPT Code(s)
81479
Components
Component Test Code*Component Chart Name
2007915EPOR Specimen Received
2007916EPOR Mutation Detection Results
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, contact interface support at interface.support@aruplab.com.
Cross References
  • EPOR Gene, Mutation Analysis