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GTR Home > Tests > Variant Resolution Test for Penn Cancer Grant Panel (+RNAinsight®)

How to order

Test Order CodeHelp: 9232-R

How To Order

Laboratory's Test Page



How To Order


Order URL Help: http://www.ambrygen.com/clinician/ordering-process

Informed Consent Required Help: Based on applicable state law

Specimen Source

  • Peripheral (whole) blood

Specimen requirements: https://www.ambrygen.com/clinician/specimen-requirements

Test Codes


Not provided

Test Orderable By

  • Genetic Counselor
  • Health Care Provider
  • Nurse Practitioner
  • Licensed Physician

Test services

  • Clinical Testing/Confirmation of Mutations Identified Previously, Order code: 5555

Ordering Requirements

Genetic Counseling Required Pre-test Help
Decline to answer
Genetic Counseling Required Post-test Help
Decline to answer

Contact Policy


Not provided

Laboratory Contact For This Test

  • Monalyn Salvador, MS, CGC, Manager, Product Management - Oncology
  • Phone Number: 949-457-8961
  • Email: mumali@ambrygen.com

Suggested reading

Practice guidelines

  • NCCN, 2023
    NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Colon Cancer, 2023
  • ACMG ACT, 2019
    American College of Medical Genetics and Genomics, Genomic Testing (Secondary Findings) ACT Sheet, APC Pathogenic Variants (Familial Adenomatous Polyposis [FAP]), 2019
  • ACMG ACT, 2012
    American College of Medical Genetics and Genomics Family History ACT Sheet, Colon Cancer (Asymptomatic), 2012
  • EuroGenetest, 2011
    Clinical utility gene card for: familial adenomatous polyposis (FAP) and attenuated FAP (AFAP).

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.