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

Please refer to Molecular Genetics - Austin Pathology for specific testing details and request form for ordering.

Usally 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.

Collection Instructions

BLOOD

  • 1 x  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