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Medical information Clinical review pending

Genetic Testing

Comprehensive Tumor Panel 320 Genes

The Comprehensive Tumor Panel 320 Genes test identifies genetic mutations in tumors, aiding oncologists in developing personalized cancer treatment strategies. This test analyzes 320 genes associated with various cancers.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
Tumor tissue (biopsy sample) is required. Formalin-fixed, paraffin-embedded (FFPE) tissue is typically preferred. Confirm specific requirements with the laboratory before sample collection.
Results
Confirm with the laboratory before booking.
Preparation
No specific patient preparation is required for this test. Ensure the tumor tissue sample is collected and preserved according to laboratory guidelines.
Test priceKSh 66,000

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the Comprehensive Tumor Panel 320 Genes test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Patients diagnosed with various types of cancer.
  • ✓Individuals seeking personalized cancer treatment options.
  • ✓Patients whose cancer may be resistant to standard therapies.
  • ✓Cases where genetic information can guide targeted therapy selection.
  • ✓Assessing potential inherited cancer risk factors (in conjunction with other tests).
02

In plain language

What this test helps you understand

This test helps identify specific genetic alterations in tumors that can inform personalized cancer treatment decisions, potentially improving outcomes and guiding therapy selection.
The Comprehensive Tumor Panel 320 Genes is an advanced diagnostic test used to identify genetic changes within tumor cells. This information is vital for oncologists to understand the specific characteristics of a patient's cancer and to guide treatment decisions. By analyzing a broad spectrum of 320 genes known to be involved in cancer development and progression, this test provides a detailed genetic profile of the tumor. This comprehensive analysis helps healthcare providers select the most effective therapies, predict potential responses to treatment, and identify possible resistance mechanisms. The test utilizes Next Generation Sequencing (NGS) technology for accurate and thorough analysis. Discussing the results with your doctor is crucial for understanding their implications for your specific situation and treatment plan.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationNo specific patient preparation is required for this test. Ensure the tumor tissue sample is collected and preserved according to laboratory guidelines.
SampleTumor tissue (biopsy sample) is required. Formalin-fixed, paraffin-embedded (FFPE) tissue is typically preferred. Confirm specific requirements with the laboratory before sample collection.
MethodologyNext Generation Sequencing (NGS) is used to analyze the DNA extracted from the tumor tissue sample.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects mutations in the 320 genes included in the panel. It may not detect all possible genetic alterations. Results are based on the quality of the submitted sample. Interpretation requires clinical correlation.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

This test looks for specific genetic mutations, deletions, or amplifications in 320 genes commonly associated with different types of cancer.
A tissue sample from the tumor, usually obtained via biopsy, is required for this test. Please consult your doctor regarding sample collection.
Confirm with the laboratory before booking.
A qualified medical professional, such as an oncologist or geneticist, will interpret the results in the context of your medical history and clinical findings.
Insurance coverage varies. Please check with your insurance provider regarding coverage for this specific test.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

Explore partnerships
09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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