ARUP's Laboratory Test Directory

WT1 Mutation Detection by Sequencing : 2005766
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Additional Technical Information
  


Mnemonic: WT1

Ordering Recommendation: WT1 testing is appropriate for detecting mutations in exons 7 and 9 as well as for the presence of SNP rs16754 in cases of cytogenetically normal AML.
Methodology: Polymerase Chain Reaction/Sequencing
Performed: Varies
Reported: 12-14 days
Specimen Required: Collect: Lavender (EDTA) OR bone marrow (EDTA).

Specimen Preparation: Transport 5 mL whole blood (Min: 1 mL) OR 3 mL bone marrow (Min: 1 mL).

Storage/Transport Temperature: Refrigerated

Unacceptable Conditions: Serum or plasma. Specimens collected in anticoagulants other than EDTA. Frozen specimens. Clotted or severely hemolyzed specimens

Stability (collection to initiation of testing): Ambient: 24 hours; Refrigerated: 5 days; Frozen: Unacceptable

Interpretive Data: Refer to report

See Compliance Statement B: www.aruplab.com/CS
CPT Code(s): 81479, G0452