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DNA Labs India

FLT3 (ITD, D835Y) Mutation Detection Test

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FLT3 (ITD, D835Y) Mutation Detection Test

Short Name: FLT3 Mutation Detection

Also known as: FLT3-ITD, FLT3-D835Y, FLT3 Mutation Test

FLT3 (ITD, D835Y) Mutation Detection Test test available at DNA Labs India for ₹6,000. Uses End Point PCR on Bone marrow / Peripheral blood samples. Results in 3-4 days. Free home collection in 300+ cities across India.

Molecular Testing🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of FLT3 mutation detection is to identify genetic mutations in the FLT3 gene that are associated with acute myeloid leukemia (AML). This test helps in diagnosing AML, determining prognosis, and guiding treatment decisions, especially for targeted therapies.

Test Code
3016
Price
₹6,000
Sample Type
Bone marrow / Peripheral blood
Result Time
3-4 days
Fasting Required
No
Method
End Point PCR
Step 1

Sample Collection

No special preparation required. Inform the doctor about any medications or recent treatments.

Method: Bone Marrow Aspiration or Venipuncture

Step 2

Laboratory Analysis

A sample of bone marrow or peripheral blood will be collected by a trained phlebotomist or hematologist.

Step 3

Report Delivery

Apply pressure to the collection site to prevent bleeding. Resume normal activities unless advised otherwise.

Timeline: 3-4 days

Patient Instructions

1
Before the Test:No fasting required. Ensure a doctor's prescription is available if needed.
2
During the Test:The test involves PCR amplification and analysis of FLT3 gene sequences from the collected sample.
3
After the Test:Results will be available in 3-4 days. Follow up with your doctor for interpretation.

About This Test

Who Should Get This Test

The purpose of FLT3 mutation detection is to identify genetic mutations in the FLT3 gene that are associated with acute myeloid leukemia (AML). This test helps in diagnosing AML, determining prognosis, and guiding treatment decisions, especially for targeted therapies.

How to Prepare

  • Use EDTA vacutainer for blood samples
  • Transport bone marrow samples immediately to the lab
  • Label samples correctly with patient details
  • Avoid hemolysis during collection

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"FLT3 mutation detection is essential for risk stratification and targeted therapy in acute myeloid leukemia. Early identification can improve treatment outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBone marrow / Peripheral blood
Sample Volume2 ml
ContainerEDTA Vacutainer
Collection MethodBone Marrow Aspiration or Venipuncture

Sample Stability

Blood samples: stable for 24 hours at room temperature
Bone marrow samples: process within 2 hours
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Incorrect sample container
  • Insufficient sample volume
  • Improper labeling

Understanding Your Results

Results indicate the presence or absence of FLT3-ITD and FLT3-D835Y mutations. Detection of these mutations is associated with a higher risk of relapse and poorer prognosis in AML.
📊

FLT3-ITD Detected

Presence of internal tandem duplication in FLT3 gene, associated with poor prognosis in AML.

📊

FLT3-D835Y Detected

Presence of D835Y point mutation in FLT3 gene, associated with poor prognosis in AML.

📊

Both Mutations Not Detected

No FLT3 mutations detected, which may indicate a better prognosis, but other factors should be considered.

⚠️ When to Consult a Doctor:

Consult a hematologist or oncologist immediately if FLT3 mutations are detected for personalized treatment planning. Also, consult if symptoms of AML persist despite negative results.

Limitations

  • May not detect all FLT3 mutations
  • False negatives possible in low tumor burden
  • Does not replace comprehensive AML genetic panel
  • Results should be correlated with clinical findings

Risks & Considerations

  • Pain or bruising at the blood draw site
  • Infection risk for bone marrow aspiration
  • Rare allergic reactions to antiseptics

Interfering Factors

  • Sample contamination
  • Improper sample storage or transport
  • Hemolyzed or clotted samples
  • Recent blood transfusion may affect results

Compare With Similar Tests

TestFLT3 (ITD, D835Y) Mutation DetectionNPM1 Mutation DetectionCEBPA Mutation DetectionRUNX1 Mutation Detection
ComparisonFLT3 (ITD, D835Y) Mutation DetectionNPM1 mutations are common in AML and often co-occur with FLT3 mutations. Combined testing provides better prognostic information.CEBPA mutations are associated with a favorable prognosis in AML, unlike FLT3 mutations.RUNX1 mutations indicate poor prognosis and may guide treatment decisions similar to FLT3.

Frequently Asked Questions

What is FLT3 mutation detection?
FLT3 mutation detection is a genetic test that identifies mutations in the FLT3 gene, commonly associated with acute myeloid leukemia (AML).
Why is FLT3 mutation testing important for AML?
It helps in prognosis assessment and guides targeted therapy, as FLT3 mutations are linked to poorer outcomes in AML.
What are the symptoms of FLT3 mutations?
FLT3 mutations themselves don't cause specific symptoms, but in AML, symptoms include fever, fatigue, weight loss, bone pain, and easy bruising.
How is the FLT3 test performed?
A bone marrow or blood sample is collected and analyzed using end-point PCR to detect FLT3-ITD and D835Y mutations.
What is the cost of FLT3 mutation detection in India?
The cost is INR 6000 at DNA Labs India, with home sample collection available across many cities.
Is home sample collection available for this test?
Yes, free home sample collection is offered for online bookings in numerous cities across India.
How long does it take to get FLT3 test results?
Results are typically available within 3-4 days after sample collection.
What does a positive FLT3 mutation result mean?
A positive result indicates the presence of FLT3 mutations, which are associated with a higher risk of relapse and poorer prognosis in AML.
Can FLT3 mutations be treated?
Yes, targeted therapies like FLT3 inhibitors are available and can be used based on mutation detection results.
Are there any risks associated with the test?
Risks are minimal and include pain or bruising at the collection site, and for bone marrow aspiration, a small risk of infection.
Do I need a doctor's prescription for this test?
Yes, a doctor's prescription is generally required, except for surgery, pregnancy cases, or travel abroad planning.
How accurate is the FLT3 mutation detection test?
The test is highly accurate using PCR technology, but results should be interpreted in conjunction with clinical findings.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

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Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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