Austin Pathology

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FLT3 & NPM1 Mutation Analysis (Blood)

Alternate Names
FLT3-ITD, FLT3-TKD
Test Code
AFLTNP
Testing Laboratory
Molecular Diagnostics - Genetics
Specimen Type

Blood

Container Type

9 mL EDTA (Purple Top)

Container Image
Medicare Rebate

Yes

Out of Pocket Costs

Please note: Medicare Rebate for this test is subject to conditions. Patients may receive an invoice:

  • Fully covered by Medicare - MBS 73314
  • Non-Medicare eligible - $230.95

Fee above is an indication only; please contact testing laboratory for up-to date cost. 

Ordering Information

Usually requested with NPM1 which has the same test code AFLTNP.

This test will detect mutations by capilliary electrophoresis in both FLT3-ITD and FLT3-TKD.

If this test is urgent,please contact Molecular Diagnostics Laboratory on 03 9496 5657.

To order, use the Molecular Haematology Request form (pricing included): Molecular Haematology Test Request Form V13

Collection Instructions

BLOOD

  • A DEDICATED 9 mL EDTA tube must be collected and should not be shared with other tests of the same sample type.

Instructions for: External Referring Laboratories

  • If DNA is the preferred specimen type, a minimum of 20μL at 50ng/μL is required.
Transport Instructions
Transport ambient at room temperature
Storage Instructions
Store refrigerated at 4°C
Testing Frequency
Twice per week
Min Test Volume
4mL
Add On Test Suitability

Contact Molecular Diagnostics - Genetics on 03 9496 5657 to confirm add on suitability.

Container ID
EW, EWL, CMOL, CMOLS
CSR Instructions

Instructions for: Metropolitan & Regional Specimen Receptions 

Instructions for: Regional Specimen Receptions

  • Forward all samples for this test to the Heidelberg Laboratory.
Laboratory Instructions
None
Accredited Test
Yes