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DNA Labs India

BRAF Mutation Analysis (V600E) Test

DNA Labs India | ISO 9001:2015 Certified

BRAF Mutation Analysis (V600E) Test

Short Name: BRAF V600E

Also known as: BRAF V600E Mutation Test, BRAF Gene Mutation Analysis

BRAF Mutation Analysis (V600E) Test test available at DNA Labs India for ₹9,000. Uses Sanger Sequencing on Tumor tissue samples. Results in 7-8 days. Free home collection in 300+ cities across India.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of BRAF Mutation Analysis (V600E) is to identify the presence of the BRAF V600E mutation in cancerous tissues, which helps in diagnosing specific cancer types, predicting response to targeted therapies, and guiding personalized treatment strategies for improved patient outcomes.

Test Code
2955
Price
₹9,000
Sample Type
Tumor tissue
Result Time
7-8 days
Fasting Required
No
Method
Sanger Sequencing
Step 1

Sample Collection

A doctor's prescription is required for BRAF Mutation Analysis (V600E). Prescription is not applicable for surgery, pregnancy cases, or people planning to travel abroad. Ensure all patient details are accurately provided.

Method: Biopsy or surgical sample

Step 2

Laboratory Analysis

Sample collection involves obtaining a tumor tissue biopsy or surgical specimen under sterile conditions by a qualified healthcare professional.

Step 3

Report Delivery

The sample is preserved and sent to the laboratory for analysis. Patients may experience minor discomfort at the biopsy site, which typically resolves quickly.

Timeline: 7-8 days

Patient Instructions

1
Before the Test:Obtain a doctor's prescription. No fasting is required. Provide accurate medical history and sample details.
2
During the Test:Sample collection is performed by a healthcare professional. The procedure is minimally invasive, similar to a biopsy.
3
After the Test:Results are available online within 7-8 days. Follow up with your doctor to discuss the findings and next steps.

About This Test

Who Should Get This Test

The purpose of BRAF Mutation Analysis (V600E) is to identify the presence of the BRAF V600E mutation in cancerous tissues, which helps in diagnosing specific cancer types, predicting response to targeted therapies, and guiding personalized treatment strategies for improved patient outcomes.

How to Prepare

  • Collect tumor tissue sample via biopsy or surgical excision
  • Use appropriate containers and fixatives as per laboratory guidelines
  • Label the sample with patient details and test information
  • Transport the sample at ambient temperature to the laboratory

Doctor's Notes

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

"Early detection of BRAF mutations can guide targeted therapy and improve patient outcomes in various cancers, including melanoma and thyroid cancer."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeTumor tissue
Collection MethodBiopsy or surgical sample

Sample Stability

Tissue samples should be processed within 24 hours of collection
Paraffin-embedded blocks can be stored at room temperature for extended periods
Sample Rejection Criteria:
  • Insufficient or non-representative tumor tissue
  • Sample contamination or improper labeling
  • Missing doctor's prescription where required

Understanding Your Results

Results of BRAF Mutation Analysis (V600E) indicate whether the BRAF V600E mutation is present in the tumor sample. A positive result suggests the cancer may respond to targeted therapies, while a negative result means the mutation is not detected.
📊

Detected

BRAF V600E mutation is present, indicating potential eligibility for targeted therapies like BRAF inhibitors.

Action: Consult with an oncologist for personalized treatment planning.

📊

Not Detected

BRAF V600E mutation is not found in the sample. Other genetic tests may be considered.

Action: Discuss alternative diagnostic or treatment options with your doctor.

⚠️ When to Consult a Doctor:

Consult a doctor if you have symptoms such as new or changing moles, skin lesions that bleed or itch, persistent cough, chest pain, or a family history of cancer. Early consultation can facilitate timely testing and treatment.

Limitations

  • Test only detects the V600E mutation; other BRAF mutations may not be identified
  • Results are dependent on the quality and representativeness of the tumor sample
  • False negatives may occur if tumor heterogeneity is present

Risks & Considerations

  • Minor pain or bleeding at the biopsy site
  • Risk of infection, though rare with proper sterile techniques
  • Possible need for repeat sampling if initial sample is inadequate

Interfering Factors

  • Poor sample quality or insufficient tissue
  • Contamination during sample collection or processing
  • Use of certain fixatives that may affect DNA integrity

Frequently Asked Questions

What is BRAF Mutation Analysis (V600E)?
It is a genetic test that detects the BRAF V600E mutation in tumor tissue, commonly associated with cancers like melanoma, colorectal, lung, and thyroid cancer.
Why is this test important?
Early detection of BRAF mutations helps in selecting targeted therapies, improving treatment effectiveness and patient outcomes in cancer care.
What is the cost of the test?
The test costs INR 9000, which includes home sample collection across India.
How is the sample collected?
A tumor tissue sample is collected via biopsy or surgical procedure by a healthcare professional.
Is fasting required for this test?
No, fasting is not required for BRAF Mutation Analysis (V600E).
How long does it take to get results?
Results are typically available within 7-8 days after sample collection.
What does a positive result mean?
A positive result indicates the presence of the BRAF V600E mutation, suggesting potential eligibility for targeted therapies like BRAF inhibitors.
What are the risks of the test?
Risks are minimal and may include minor pain or bleeding at the biopsy site, with rare chances of infection.
Is the test covered by insurance?
Coverage varies by insurance plan. It is recommended to check with your provider for specific details.
Can I get home sample collection?
Yes, DNA Labs India offers free home sample collection for online bookings across many cities in India.
What should I do before the test?
Obtain a doctor's prescription and provide accurate medical history. No special preparation is needed.
How accurate is the test?
The test uses Sanger Sequencing, a highly accurate method, but results depend on sample quality and tumor representativeness.
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.

LIMS Integration

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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