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DNA Labs India

NRAS Gene NRAS, selective sequencing of exons 2 and 3 NGS Genetic Test

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NRAS Gene NRAS, selective sequencing of exons 2 and 3 NGS Genetic Test

NRAS Gene NRAS, selective sequencing of exons 2 and 3 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

Next-Generation Sequencing (NGS)🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify mutations in exons 2 and 3 of the NRAS gene, which are associated with an increased risk of various cancers, aiding in diagnosis and treatment planning.

Test Code
2917
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

Provide clinical history of the patient. A genetic counseling session is recommended to draw a pedigree chart of family members affected with NRAS gene mutations.

Step 2

Laboratory Analysis

Your sample is analyzed using NGS Technology in our laboratory.

Step 3

Report Delivery

A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling and review of clinical history are recommended before the test.

About This Test

Who Should Get This Test

To identify mutations in exons 2 and 3 of the NRAS gene, which are associated with an increased risk of various cancers, aiding in diagnosis and treatment planning.

How to Prepare

  • Collect blood sample in appropriate container.
  • Alternatively, use extracted DNA or one drop of blood on FTA card.
  • Ensure proper labeling and handling of the sample.

Doctor's Notes

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

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card

Understanding Your Results

Results of the NRAS Gene Sequencing Test indicate the presence or absence of mutations in exons 2 and 3. Interpretation should be done by a qualified healthcare professional.
📊

Negative

No mutations detected in exons 2 and 3 of the NRAS gene. This suggests a lower risk of NRAS-associated cancers, but clinical correlation is advised.

📊

Positive

Mutations detected in exons 2 and/or 3 of the NRAS gene. This may indicate an increased risk of certain cancers and warrants further clinical evaluation and management.

⚠️ When to Consult a Doctor:

Consult a doctor if you experience symptoms such as skin changes, blood in stools or urine, abdominal pain, trouble breathing, or unexplained weight loss, especially with a family history of cancer.

Risks & Considerations

  • Minimal physical risks from blood draw.
  • Potential psychological impact from test results.

Frequently Asked Questions

What is the NRAS Gene Sequencing Test?
It is a genetic test that uses NGS technology to detect mutations in exons 2 and 3 of the NRAS gene, associated with cancer risk.
Who should take this test?
Individuals with symptoms of cancer, family history of NRAS mutations, or those diagnosed with melanoma, colorectal, or thyroid cancer.
What sample is required?
Blood, extracted DNA, or one drop of blood on an FTA card.
Is fasting required?
No, fasting is not required for this test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks.
What is the cost of the test?
The test costs INR 20,000 at DNA Labs India.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across India.
What does a positive result mean?
A positive result indicates mutations in the NRAS gene, which may increase cancer risk and require further medical evaluation.
What does a negative result mean?
A negative result means no mutations were detected in exons 2 and 3, suggesting lower risk, but clinical correlation is advised.
Are there any risks associated with the test?
Risks are minimal, mainly related to blood draw, but psychological impact of results should be considered.
How is the test performed?
The test uses next-generation sequencing (NGS) to analyze specific exons of the NRAS gene.
Can this test be used for treatment planning?
Yes, identifying NRAS mutations can help doctors develop personalized treatment plans for cancer patients.
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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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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