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NRAS Mutation Analysis

The NRAS mutation analysis test is a genetic test designed to identify mutations in the NRAS gene. These mutations are commonly observed in various forms of cancer, including melanoma, colorectal cancer, and some types of leukemia. The presence of an NRAS mutation can influence a patient's prognosis and guide treatment decisions.


  • Profile Name: NRAS Mutation Analysis
  • Sample Type: Tissue
  • Preparations Required: Before undergoing this test, make sure to discuss with your doctor any medications or supplements you are currently taking, as certain substances can interfere with the results.
  • Report Time: 7 days

The NRAS gene is responsible for the production of a protein that helps control cell growth and division. When mutated, this gene can lead to the development of cancerous cells, as it promotes abnormal and uncontrolled cell growth.

Home Sample Collection Process
1
Book your convenient slot
Book your convenient slot
2
Sample Collection by Phlebotomist
Sample Collection by Phlebotomist
3
Reporting of the sample at lab
Reporting of the sample at lab
4
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Frequently Asked Questions

Your doctor might recommend an NRAS mutation analysis if you have been diagnosed with a type of cancer where NRAS mutations are common, such as melanoma, colorectal cancer, or certain types of leukemia. The test can guide treatment decisions and provide information on your prognosis.

The test is performed on a sample of your tissue or blood. The DNA in the sample is extracted and analyzed for the presence of mutations in the NRAS gene.

The test involves either a blood draw or a biopsy to collect a tissue sample, both of which carry minimal risks. Risks can include minor pain or bruising at the site of the needle insertion, light-headedness, or, in rare cases, infection.

A positive result means that a mutation in the NRAS gene has been detected. This result can provide insight into the best course of treatment and your overall prognosis.

Yes, the test can be performed on individuals of any age, although cancers with NRAS mutations are more commonly diagnosed in adults.

The presence of an NRAS mutation can guide treatment decisions. For instance, certain targeted therapies work specifically on cancers with this mutation. Therefore, knowing your mutation status can help your doctor personalize your treatment.

Most NRAS mutations linked to cancer are not inherited but are instead acquired during a person's lifetime. They exist only in the cancer cells.

The test is highly accurate when performed in a qualified laboratory. However, no test is perfect. There may be instances where a mutation is present but not detected, or vice versa.

The typical turnaround time for the NRAS mutation analysis test is between 10 and 14 days, but it can vary depending on the lab.

Yes, there are typically no specific dietary restrictions before the test. However, it's always best to follow the instructions provided by your healthcare provider.

If your test results are positive, your healthcare provider will discuss the implications with you. The presence of an NRAS mutation may influence your treatment plan and provide more information about your prognosis.

While the primary purpose of this test is to detect NRAS mutations in the context of certain cancers, it's not typically used to diagnose other conditions.

While this test is highly accurate, it may not detect all NRAS mutations. Additionally, some mutations may have an unclear significance. As such, results should be interpreted in the context of the patient's overall clinical picture.

No, this test requires a sample to be collected by a healthcare professional and sent to a specialized lab for analysis.

In summary, the NRAS mutation analysis test is an essential tool in diagnosing and managing certain cancers. The information it provides can influence your treatment plan and help your healthcare provider give you the most effective care. If you have been diagnosed with a relevant type of cancer, it's worth discussing this test with your healthcare provider.

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