NRAS Mutation AnalysisPrint this page
Updated Test Information:
NRAS Mutation Analysis
NRAS Gene Sequencing, NRAS Exons 2-4
Bi-directional sequencing of NRAS exons 2, 3, and 4 including codons 12, 13, 59, 61, 117, and 146.
NRAS is highly homologous with KRAS; both are members of the most frequently mutated family of oncogenes. NRAS mutations are found in a wide variety of solid tumors, in advanced systemic mastocytosis, and in myeloid neoplasias. Patients with any known KRAS mutation or NRAS mutation may be resistant to certain tyrosine kinase inhibitors. Testing is available separately or in combination with BRAF, HRAS and KRAS in the RAS/RAF Panel.
FFPE solid tumor tissue: Paraffin block is preferred. Alternatively, send 1 H&E slide plus 5-10 unstained slides cut at 5 or more microns. Please use positively-charged slides and 10% NBF fixative. Do not use zinc fixatives.
Complete the Incyte Diagnostics requisition with the patient's demographics and relevant clinical history.
Use cold pack for transport, making sure cold pack is not in direct contact with specimen.
Extracted DNA is kept for 30 days.