NRAS EXON 2 AND 3 MUTATION, TISSUE

This test identifies mutations in exons 1 and 2 of the NRAS gene, which are implicated in various cancers like melanoma and leukemia. It helps in guiding targeted therapy decisions for cancer treatment.

Also known asNras Exon 1 And 2 Mutation Nras Exon 1 And 2 Mutation

Available via

Home Collection, Lab Visit

Contains

4 parameters

Earliest reports in

7 Working Days

Test details

NRAS EXON 2 AND 3 MUTATION, TISSUE Test in Bengaluru Overview

What is NRAS Exon 1 and 2 mutation test?

NRAS Exon 1 and 2 mutation test detects mutations in the NRAS gene, specifically in exons 1 and 2, which code for parts of the NRAS protein involved in cell growth and division. Mutations in NRAS gene can lead to uncontrolled cell signaling, contributing to the development of various cancers such as melanoma, colorectal cancer, leukemia, and thyroid cancer. NRAS Exon 1 and 2 mutation test helps identify whether such mutations are present in a patient’s tumor or blood sample.

Why consider NRAS Exon 1 and 2 mutation test?

NRAS Exon 1 and 2 mutation test can be considered

  • To guide targeted therapy decisions as certain cancer treatments work better (or worse) depending on NRAS mutation status.
  • To help in prognosis and disease characterization as NRAS mutations may indicate how aggressive a cancer is.
  • To differentiate between similar cancers with different genetic drivers.
  • To monitor disease progression or recurrence in patients with known NRAS-mutant tumors.

Who should get tested for NRAS Exon 1 and 2 mutation test

NRAS Exon 1 and 2 mutation test is generally recommended for:

  • Patients diagnosed with metastatic or advanced colorectal cancer to determine eligibility for anti-EGFR therapy.
  • Individuals with melanoma or hematologic malignancies to identify targeted treatment options.
  • Patients whose oncologist suspects a RAS pathway–driven cancer.
  • Those being evaluated for molecular profiling of tumors as part of personalized medicine.

More Information

Other Names: NRAS Gene Mutation Test, NRAS Molecular Analysis (Exons 1 & 2), NRAS Mutation Detection by PCR/Sequencing

The NRAS protein is a small GTPase that acts as a molecular switch in signal transduction pathways, relaying signals from outside the cell to the nucleus to regulate cell growth, division, and differentiation. It is encoded by the NRAS gene and is a member of the Ras family of proto-oncogenes, meaning that mutations in the gene can contribute to the development of cancer. Mutations in the NRAS gene have been linked to various diseases, including several types of cancer, as well as certain congenital disorders.  

Preparations

No special preparations needed

Test included
NRAS EXON 2 AND 3 MUTATION, TISSUE includes 4 parameters

  • Preliminary Report
  • Nras Exon 2 And 3 Mutation
  • Block Identification Number
  • Clinical Details

Test code

RD1316

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
TissueOthers1 NOS

Specimen stability information

Tissue

Collection instructions

Site Of Biopsy & Clinical Details Mandatory If Tissue Recd.

Specimen rejection criteria

Test run frequency

Every Day TIME - 09:30

Turn around time

7 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

NRAS EXON 2 AND 3 MUTATION, TISSUE

6500