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What is a BRAF V600 MUTATION DETECTION?

The BRAF V600 Mutation Detection test is a molecular diagnostic test used to identify mutations in the BRAF gene, specifically at codon V600. This mutation leads to abnormal activation of the MAPK signaling pathway, driving uncontrolled cell growth in cancers such as melanoma, colorectal cancer, and thyroid cancer. Detecting the BRAF V600 mutation is crucial for guiding targeted therapy decisions, predicting prognosis, and selecting patients who may benefit from specific treatments like BRAF inhibitors or immunotherapy.

Additional Information

Also known as/ Other names: BRAF V600E Mutation Test, BRAF Mutation Analysis, BRAF Gene Mutation Detection, BRAF Molecular Testing
Parameters: 1
Recommended for: M/F/Others
Sample Type: FFPE Tissue block
Patient Preparation: No prior preparation is needed
Reports: 5 days

FAQs

Why is this test important?

It helps healthcare profession targets therapy decisions, predict prognosis, and identify patients who may benefit from BRAF inhibitors or immunotherapy.

Who should undergo this test?

Patients with melanoma, colorectal cancer, thyroid cancer, or other tumors suspected of harboring BRAF mutations are recommended for testing.

What happens if the test is positive?

A positive result indicates the presence of BRAF V600 mutation, guiding targeted therapy options.

What does a negative result mean?

It suggests no detectable BRAF V600 mutation in the tested tumor sample.

Can medications affect the test results?

No, medications do not interfere with genetic mutation detection.

Is this test safe for children?

Yes, it is safe if clinically indicated, using tumor tissue samples.

What are the risks of not testing?

Without testing, patients may miss opportunities for personalized treatment with targeted therapies.

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