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CEBPA Mutation Detection Test

DNA Labs India | ISO 9001:2015 Certified

CEBPA Mutation Detection Test

Short Name: CEBPA Mutation Detection

Also known as: CEBPA Gene Mutation Test, CEBPA Genetic Test

CEBPA Mutation Detection Test test available at DNA Labs India for ₹10,000. Uses PCR on Whole blood samples. Results in Reports available within 10 working days after sample receipt.. Free home collection in 300+ cities across India.

PCR-based Genetic TestAdults🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the CEBPA Mutation Detection Test is to identify mutations in the CEBPA gene, which can indicate a risk for or presence of acute myeloid leukemia (AML) and related blood disorders. Detection helps in confirming diagnosis, guiding treatment strategies such as targeted therapies, and monitoring disease progression.

Test Code
278
Price
₹10,000
Sample Type
Whole blood
Result Time
Reports available within 10 working days after sample receipt.
Fasting Required
No
Method
PCR
Step 1

Sample Collection

Ensure the Genomics Clinical Information Requisition Form (Form 20) is filled out accurately. No fasting required.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample of 4 mL is drawn from a vein into a lavender top EDTA tube. The process is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding. Sample is shipped refrigerated; do not freeze.

Timeline: Reports available within 10 working days after sample receipt.

Patient Instructions

1
Before the Test:No specific preparation needed. Ensure the requisition form is completed.
2
During the Test:Blood sample collection via venipuncture, typically taking a few minutes.
3
After the Test:Mild discomfort at puncture site possible. Resume normal activities immediately.

About This Test

Who Should Get This Test

The purpose of the CEBPA Mutation Detection Test is to identify mutations in the CEBPA gene, which can indicate a risk for or presence of acute myeloid leukemia (AML) and related blood disorders. Detection helps in confirming diagnosis, guiding treatment strategies such as targeted therapies, and monitoring disease progression.

How to Prepare

  • Collect 4 mL whole blood in lavender top (EDTA) tube.
  • Ship refrigerated, do not freeze.
  • Include the completed Genomics Clinical Information Requisition Form (Form 20).

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Early detection of CEBPA mutations can guide treatment decisions in acute myeloid leukemia, improving patient outcomes."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeWhole blood
Sample Volume4 mL (2 mL min.)
ContainerLavender top (EDTA) tube
Collection MethodVenipuncture

Sample Stability

Room TemperatureNot Applicable
Refrigerator1 week
FrozenNot Applicable
Sample Rejection Criteria:
  • Sample not collected in specified container.
  • Missing or incomplete requisition form.
  • Sample frozen or hemolyzed.

Understanding Your Results

Results indicate whether mutations are detected in the CEBPA gene. A positive result suggests a higher risk for leukemia, while a negative result indicates no mutations found, but does not rule out other conditions.
📊

Negative

No CEBPA mutations detected. Clinical correlation is recommended as symptoms may be due to other causes.

📊

Positive

CEBPA mutation detected. This is associated with acute myeloid leukemia and may require further evaluation and targeted treatment.

⚠️ When to Consult a Doctor:

Consult a doctor if you experience symptoms like unexplained weight loss, persistent fever, fatigue, bone pain, bruising, frequent infections, or anemia. A healthcare provider can recommend this test based on clinical assessment.

Limitations

  • Test may not detect all possible CEBPA mutations.
  • Results should be interpreted in conjunction with clinical findings.

Risks & Considerations

  • Minor bruising or pain at puncture site.
  • Rare risk of infection or dizziness.

Frequently Asked Questions

What is the CEBPA Mutation Detection Test?
It is a genetic test that identifies mutations in the CEBPA gene, linked to acute myeloid leukemia and blood disorders.
What are the symptoms that indicate the need for this test?
Symptoms include unexplained weight loss, fever, fatigue, bone pain, easy bruising, frequent infections, and anemia.
How is the test performed?
A blood sample is collected and analyzed using PCR technology to detect CEBPA gene mutations.
What is the cost of the CEBPA Mutation Detection Test?
The test costs INR 10000.0, with home collection available across India.
Is fasting required for this test?
No, fasting is not required, but a completed requisition form is mandatory.
How long does it take to get results?
Reports are typically available within 10 working days after sample collection.
What does a positive result mean?
A positive result indicates the presence of CEBPA mutations, which may be associated with leukemia. Consult a doctor for further evaluation.
What if the result is negative?
A negative result means no mutations were detected, but symptoms should be discussed with a healthcare provider as other conditions may exist.
Can I get home collection for this test?
Yes, free home sample collection is available for online bookings in many cities across India.
What other tests might be needed alongside this one?
Other tests like CBC, bone marrow biopsy, or flow cytometry may be recommended for comprehensive diagnosis.
Is this test covered by insurance?
Coverage varies by insurance scheme. It is generally not covered under government schemes; check with your provider.
Who should I consult for interpreting the results?
Consult an oncologist or hematologist for result interpretation and treatment planning.
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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