NPM1+ CEBPA Test
NPM1+ CEBPA Test test available at DNA Labs India for ₹13,500. 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+ CEBPA test is to identify genetic mutations in the NPM1 and CEBPA genes, which are biomarkers for various blood disorders, including leukemia. This test aids in accurate diagnosis, prognosis assessment, and treatment planning for patients with suspected hematological conditions.
- Test Code
- 3114
- Price
- ₹13,500
- Sample Type
- Bone marrow / Peripheral blood
- Result Time
- 7-8 days
- Fasting Required
- No
- Method
- Sanger Sequencing
Sample Collection
A doctor's prescription is required for the NPM1+ CEBPA test. Prescription is not applicable for surgery, pregnancy cases, or individuals planning to travel abroad. Ensure the sample is transported immediately after collection.
Method: Venipuncture or bone marrow aspiration
Laboratory Analysis
Sample collection involves venipuncture for peripheral blood or bone marrow aspiration. The process is performed by trained phlebotomists or medical professionals.
Report Delivery
After collection, the sample is placed in an EDTA vacutainer and transported to the laboratory with a cool pack to maintain stability.
Timeline: 7-8 days
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the NPM1+ CEBPA test is to identify genetic mutations in the NPM1 and CEBPA genes, which are biomarkers for various blood disorders, including leukemia. This test aids in accurate diagnosis, prognosis assessment, and treatment planning for patients with suspected hematological conditions.
How to Prepare
- Use EDTA vacutainer for sample collection
- Transport sample immediately to the laboratory
- Maintain sample at recommended temperature during transport
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for identifying genetic mutations in blood disorders, aiding in personalized treatment plans."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Improperly labeled samples
Understanding Your Results
Detected
Mutation present; associated with increased risk of leukemia or other blood disorders. Consult a hematologist for further evaluation.
Not Detected
No mutation detected; does not rule out other conditions. Clinical correlation is recommended.
Consult a doctor if you experience symptoms such as persistent fatigue, fever, easy bruising, or swollen lymph nodes, or if you have a family history of blood disorders.
Limitations
- ⚠Test may not detect all genetic variants
- ⚠Results should be correlated with clinical findings
- ⚠Not a standalone diagnostic tool
Risks & Considerations
- ●Minor pain or bruising at the collection site
- ●Rare risk of infection
- ●Bone marrow aspiration may cause discomfort
Interfering Factors
- ●Sample contamination
- ●Improper sample storage or transport
- ●Recent blood transfusions
Frequently Asked Questions
What is the NPM1+ CEBPA test?
What is the cost of the NPM1+ CEBPA test?
What symptoms indicate the need for this test?
How is the test performed?
What is the turnaround time for results?
Is fasting required for this test?
Can this test diagnose all types of leukemia?
Is home sample collection available?
What should I do if the test is positive?
Are there any risks associated with the test?
How accurate is the NPM1+ CEBPA test?
Do I need a doctor's prescription for this test?
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