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DNA Labs India

Extended AML Panel (BCR/ABL,AML/ETO, CBFB, PML/RARA, FLT3, NPM1, CEBPA) Test

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Extended AML Panel (BCR/ABL,AML/ETO, CBFB, PML/RARA, FLT3, NPM1, CEBPA) Test

Short Name: Extended AML Panel

Also known as: AML Genetic Panel, Leukemia Mutation Panel

Extended AML Panel (BCR/ABL,AML/ETO, CBFB, PML/RARA, FLT3, NPM1, CEBPA) Test test available at DNA Labs India for ₹27,000. Uses Sanger Sequencing on Bone marrow / Peripheral blood samples. Results in 7-8 days from sample collection. Free home collection in 300+ cities across India.

Molecular Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Extended AML Panel is to detect genetic mutations in genes such as BCR/ABL, AML/ETO, CBFB, PML/RARA, FLT3, NPM1, and CEBPA, which are associated with Acute Myeloid Leukemia. This helps in confirming diagnosis, determining prognosis, guiding targeted therapy, monitoring treatment efficacy, and identifying potential relapse.

Test Code
2994
Price
₹27,000
Sample Type
Bone marrow / Peripheral blood
Result Time
7-8 days from sample collection
Fasting Required
No
Method
Sanger Sequencing
Step 1

Sample Collection

No specific preparation required. Ensure a doctor's prescription is available if needed.

Method: Venipuncture

Step 2

Laboratory Analysis

Sample collected via venipuncture from bone marrow or peripheral blood. Transport immediately to lab.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Resume normal activities unless advised otherwise.

Timeline: 7-8 days from sample collection

Patient Instructions

1
Before the Test:Obtain a doctor's prescription if required. No fasting needed. Inform the lab of any recent treatments or transfusions.
2
During the Test:Sample collection takes a few minutes via blood draw or bone marrow aspiration. Minimal discomfort expected.
3
After the Test:Results are available online in 7-8 days. Follow up with your doctor for next steps based on findings.

About This Test

Who Should Get This Test

The purpose of the Extended AML Panel is to detect genetic mutations in genes such as BCR/ABL, AML/ETO, CBFB, PML/RARA, FLT3, NPM1, and CEBPA, which are associated with Acute Myeloid Leukemia. This helps in confirming diagnosis, determining prognosis, guiding targeted therapy, monitoring treatment efficacy, and identifying potential relapse.

How to Prepare

  • Use EDTA Vacutainer (2ml) for sample collection.
  • Transport sample immediately to maintain stability.
  • Ensure proper labeling and documentation.
  • Home collection available with cool pack for preservation.

Doctor's Notes

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

"This panel is crucial for accurate diagnosis, prognosis, and personalized treatment planning in Acute Myeloid Leukemia, helping to identify specific mutations that guide therapy decisions."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBone marrow / Peripheral blood
Sample Volume2 ml
ContainerEDTA Vacutainer
Collection MethodVenipuncture

Sample Stability

Bone marrow: Stable for 24 hours at 2-8°C
Peripheral blood: Stable for 48 hours at 2-8°C
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improper container or labeling
  • Delayed transport beyond stability period

Understanding Your Results

Results from the Extended AML Panel indicate the presence or absence of specific genetic mutations. Positive results for certain mutations may guide treatment choices, while negative results may suggest other diagnostic avenues. Always consult a healthcare professional for interpretation.
📊

Mutation Detected

Presence of a specific mutation (e.g., FLT3, NPM1) may influence prognosis and therapy, such as targeted drugs.

📊

No Mutation Detected

Absence of tested mutations does not rule out AML; other genetic or cytogenetic abnormalities may be present.

📊

Fusion Gene Positive

Fusion genes like BCR/ABL or PML/RARA indicate specific AML subtypes with distinct treatment protocols.

⚠️ When to Consult a Doctor:

Consult a hematologist or oncologist if you experience symptoms of AML, have abnormal blood test results, or need guidance on treatment based on panel findings.

Limitations

  • May not detect all rare or novel mutations
  • Requires expert interpretation by geneticists
  • Results should be correlated with clinical findings and other tests
  • False negatives possible in low mutation burden cases

Risks & Considerations

  • Minor pain or bruising at puncture site
  • Rare risk of infection with bone marrow biopsy
  • No significant risks for blood draw

Interfering Factors

  • Sample contamination
  • Improper sample storage or transport
  • Recent blood transfusions affecting DNA quality
  • Technical errors in sequencing

Compare With Similar Tests

TestExtended AML Panel (BCR/ABL,AML/ETO, CBFB, PML/RARA, FLT3, NPM1, CEBPA)Complete Blood Count (CBC)Bone Marrow BiopsyCytogenetic AnalysisFLT3 Single Gene Test
ComparisonExtended AML Panel (BCR/ABL,AML/ETO, CBFB, PML/RARA, FLT3, NPM1, CEBPA)

Frequently Asked Questions

What is the Extended AML Panel test?
It is a genetic test that analyzes DNA for mutations in genes like BCR/ABL, AML/ETO, CBFB, PML/RARA, FLT3, NPM1, and CEBPA, which are associated with Acute Myeloid Leukemia.
Who should take this test?
Individuals with symptoms of AML, such as fatigue, frequent infections, or easy bruising, or those diagnosed with AML for prognosis and treatment planning.
What is the cost of the Extended AML Panel?
The test costs INR 27,000 at DNA Labs India, including home collection and result interpretation.
How is the sample collected?
A blood or bone marrow sample is collected via venipuncture and transported immediately to the lab in an EDTA vacutainer.
Is fasting required for this test?
No, fasting is not required for the Extended AML Panel test.
How long does it take to get results?
Results are typically available within 7-8 days after sample collection.
What do the results mean?
Results indicate the presence or absence of specific mutations, which help in diagnosis, prognosis, and treatment decisions. Always consult a doctor for interpretation.
Can this test detect all types of AML?
It detects common mutations but may not identify all genetic abnormalities; additional tests might be needed.
Is home collection available?
Yes, DNA Labs India offers free home sample collection across many cities in India.
What is the turnaround time for reports?
Reports are delivered in 7-8 days via online portal, email, or WhatsApp.
Do I need a doctor's prescription for this test?
A doctor's prescription is generally required, except for surgery, pregnancy, or travel abroad cases.
How accurate is the Extended AML Panel?
The test uses Sanger Sequencing, which is highly accurate for detecting specified mutations, but results should be correlated 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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