Test ID NBLD0570 JAK2 Exon 12 and Other Non-V617F Mutation Detection, Bone Marrow
Useful For
Second-order testing to aid in the distinction between a reactive cytosis and a myeloproliferative neoplasm, particularly when a diagnosis of polycythemia is being entertained; for use with bone marrow specimens
Specimen Type
Bone MarrowOrdering Guidance
In all cases being evaluated for JAK2 mutation status, the initial test that should be ordered is JAK2M / JAK2 V617F Mutation Detection, Bone Marrow, a sensitive assay for detection of the mutation. However, if no JAK2 V617F mutation is found, further evaluation of JAK2 may be clinically indicated.
This test is a second-order test that should be ordered when the test for the JAK2M / JAK2 V617F Mutation Detection, Bone Marrow test is negative.
Shipping Instructions
1. Specimen must arrive within 5 days (120 hours) of collection.
2. Draw and package specimen as close to shipping time as possible.
Necessary Information
Date of collection is required.
Specimen Required
Container/Tube:
Preferred: EDTA (lavender top)
Acceptable: ACD (yellow top)
Specimen Volume: 4 mL
Collection Instructions:
1. Invert several times to mix bone marrow.
2. Send specimen in original tube.
Specimen Minimum Volume
2 mL
Reject Due To
Gross hemolysis | Reject |
Other | Moderately to severely clotted |
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Bone Marrow | Refrigerated (preferred) | 5 days | PURPLE OR PINK TOP/EDTA |
Ambient | 5 days | PURPLE OR PINK TOP/EDTA |
Day(s) Performed
Monday through Friday
Report Available
5 to 8 daysMethod Name
Mutation Detection in cDNA Using Sanger Sequencing
Performing Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
0027U-JAK2 (Janus kinase 2) (eg, myeloproliferative disorder), exon 12 sequence and exon 13 sequence, if performed
Reporting Name
JAK2 Exon 12 Mutation Detection, BMTesting Algorithm
This is a second-order test that should be used when the test for the JAK2M / JAK2 V617F Mutation Detection, Bone Marrow test is negative.
See Myeloproliferative Neoplasm: A Diagnostic Approach to Bone Marrow Evaluation in Special Instructions.
Special Instructions
Reference Values
An interpretive report will be provided.
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.Secondary ID
60025Forms
1. Hematopathology Patient Information (T676) in Special Instructions
2. If not ordering electronically, complete, print, and send a Hematopathology/Cytogenetics Test Request (T726) with the specimen.
SANFORD INTERFACE BUILD INFORMATION
Result Code | Result Code Description |
---|---|
21732 | JAK2 Sequencing Result |
21733 | Final Diagnosis |