NPM1+FLT3+CEBPA Test
Short Name: NPM1+FLT3+CEBPA Genetic Test
Also known as: AML Genetic Panel, NPM1 FLT3 CEBPA Mutation Test
NPM1+FLT3+CEBPA Test test available at DNA Labs India for ₹19,500. Uses Sanger Sequencing on Bone marrow / Peripheral blood samples. Results in 7-8 days. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The purpose of the NPM1+FLT3+CEBPA genetic test is to identify mutations in the NPM1, FLT3, and CEBPA genes to diagnose acute myeloid leukemia (AML) and guide treatment decisions. It aids in risk stratification and personalized medicine for AML patients.
- Test Code
- 3120
- Price
- ₹19,500
- Sample Type
- Bone marrow / Peripheral blood
- Result Time
- 7-8 days
- Fasting Required
- No
- Method
- Sanger Sequencing
Sample Collection
No specific preparation required. Inform the doctor about any medications or recent procedures.
Method: Blood draw or bone marrow aspiration
Laboratory Analysis
Sample collection involves a blood draw or bone marrow aspiration by a trained professional.
Report Delivery
Apply pressure to the collection site to prevent bleeding. Keep the area clean.
Timeline: 7-8 days
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the NPM1+FLT3+CEBPA genetic test is to identify mutations in the NPM1, FLT3, and CEBPA genes to diagnose acute myeloid leukemia (AML) and guide treatment decisions. It aids in risk stratification and personalized medicine for AML patients.
How to Prepare
- Ensure proper identification of the patient
- Use sterile equipment for sample collection
- Transport the sample immediately to the lab
- Maintain sample at recommended temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This genetic test is essential for accurate diagnosis of AML and helps in tailoring personalized treatment plans for patients."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Hemolyzed or contaminated sample
- Improper labeling
- Delayed sample delivery
Understanding Your Results
Mutation detected in one or more genes
Positive for genetic mutations associated with AML. Consult an oncologist for further evaluation and treatment planning.
No mutations detected
Negative for the tested mutations. However, clinical correlation is necessary as other genetic factors may be involved.
Inconclusive result
Repeat testing or additional genetic tests may be recommended.
If you experience symptoms of AML such as persistent fatigue, unexplained bleeding, or frequent infections, consult a doctor immediately. Also, consult if you have a family history of blood cancers.
Limitations
- ⚠Only detects mutations in NPM1, FLT3, and CEBPA genes
- ⚠May not detect all genetic variants associated with AML
- ⚠Requires high-quality DNA sample
- ⚠Results should be interpreted in conjunction with clinical findings
Risks & Considerations
- ●Minor pain or bruising at the collection site
- ●Rare risk of infection
- ●For bone marrow aspiration, slight risk of bleeding or discomfort
Interfering Factors
- ●Sample contamination
- ●Improper sample storage
- ●Recent blood transfusion
- ●Use of certain medications that affect DNA
Frequently Asked Questions
What is the NPM1+FLT3+CEBPA genetic test?
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Is home sample collection available?
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Related Tests
Reference Laboratory Services
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.
Your Data Privacy
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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