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What is a NRAS MUTATION CODON 12,13 & 61?

The NRAS Mutation Codon 12, 13 & 61 test is a molecular diagnostic test that detects mutations in the NRAS gene, commonly associated with certain cancers such as melanoma, colorectal cancer, and acute myeloid leukemia. These mutations can drive abnormal cell growth and influence treatment response. The test is performed to identify the presence of NRAS mutations, guide targeted therapy decisions, and help doctors personalize cancer management by predicting prognosis and treatment effectiveness.

Additional Information

Also known as/ Other names: NRAS Mutation Analysis, NRAS Codon 12/13/61 Mutation Test, NRAS Gene Mutation Panel, NRAS Molecular Mutation 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 identify genetic mutations driving cancer growth, guiding targeted therapy decisions and predicting treatment response.

Who should undergo this test?

Patients diagnosed with melanoma, colorectal cancer, or acute myeloid leukemia may be recommended for testing.

What happens if the test is positive?

A positive result indicates NRAS mutations, which may influence treatment planning and prognosis.

What does a negative result mean?

A negative result suggests no detectable NRAS mutations in the tested codons.

Can medications affect the test results?

No, medications do not interfere with genetic mutation detection.

What are the risks of not testing?

Without testing, treatment may not be personalized, reducing effectiveness in managing cancer.

How often should the test be repeated?

It is usually done once per cancer diagnosis, unless new tissue samples are needed.

Can NRAS mutations be prevented?

No, they are genetic changes, but early detection helps guide treatment.

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