Test Entry - Detail

Detection of Somatic Variants in the NRAS Gene


General
  Clinical Use: Activation of the NRAS oncogene is implicated in various human tumours. Approximately 18% of melanomas and 3-4% of colorectal cancers (CRC) have an activating variant in NRAS. The large majority (~87%) of activating NRAS variants occur in codon 61 of exon 3, with rare variants also seen in codons 12 and 13 of exon 2 and codon 59 of exon 3 and codons 117 and 146 of exon 4. The presence of NRAS activating variant is a prognostic marker in melanoma and in patients with metastatic colorectal it is a negative predictor of response to anti-EGFR monoclonal antibody therapy. This test is Medicare rebateable for metastatic colorectal cancer (stage IV).
  Availability: Samples are tested routinely during the testing laboratory's hours of operation.
Please contact testing laboratory for urgent requests.
  Aliases/Synonyms: Neuroblastoma RAS Viral Oncogene,  
  Code: HST
  Handling Instructions (to laboratory): Contact testing laboratory for specific transport instructions.
  Hyperlink:
  Reference Interval:
Not Applicable


Collection Requirements
  Container: Sterile Container (STERILE),  
  Sample Type: Formalin Fixed or FFPE Tissue; Fresh/Frozen Tissue; Bone Marrow Trephine; Bone Marrow Aspirate; Cytological Fluid Samples; FNA
  Minimum Collection Volume: N/A
  Collection Instructions: Contact testing laboratory for specific collection instructions.


Processing Requirements
  Alternate Containers:
  Processing Instructions:
  Minimum Assay Volume: N/A
  Stability: Dependent on sample type
  Transport Instructions (to testing laboratory): Contact testing laboratory for specific transport instructions.


Testing Locations
  Performed at:
Section Department Site Contact Phone
Molecular Anatomical Pathology QEII Medical Centre 6457 2679


Last Updated : 12-11-2020 17:21