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DNA Labs India

Colon Cancer comprehensive panel NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

Colon Cancer comprehensive panel NGS Genetic Test

Short Name: Colon Cancer NGS Panel

Also known as: Colon Cancer Genetic Panel, Colorectal Cancer NGS Test

Colon Cancer comprehensive panel NGS Genetic Test test available at DNA Labs India for ₹35,000. Uses NGS Technology on Blood, Extracted DNA, or One drop Blood on FTA Card samples. Results in 3 to 4 weeks. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Colon Cancer Comprehensive Panel NGS Genetic Test is to detect genetic mutations associated with colon cancer for early diagnosis, risk assessment, and personalized treatment planning. It helps identify individuals at high risk, guides surveillance strategies, and informs therapeutic decisions.

Test Code
2832
Price
₹35,000
Sample Type
Blood, Extracted DNA, or One drop Blood on FTA Card
Result Time
3 to 4 weeks
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

Provide clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of family members affected with colon cancer or related conditions.

Method: Venipuncture for blood sample or provided DNA sample

Step 2

Laboratory Analysis

A blood sample will be collected via venipuncture, or an extracted DNA sample or one drop of blood on an FTA card can be provided.

Step 3

Report Delivery

The sample is sent to the laboratory for NGS analysis, and reports are generated within 3 to 4 weeks.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling and review of clinical and family history are recommended before sample collection.
2
During the Test:Sample collection (blood or DNA) and submission to the laboratory for NGS analysis.
3
After the Test:Report generation within 3 to 4 weeks, followed by consultation with a healthcare provider to discuss results.

About This Test

Who Should Get This Test

The purpose of the Colon Cancer Comprehensive Panel NGS Genetic Test is to detect genetic mutations associated with colon cancer for early diagnosis, risk assessment, and personalized treatment planning. It helps identify individuals at high risk, guides surveillance strategies, and informs therapeutic decisions.

How to Prepare

  • Ensure patient provides accurate clinical and family history
  • Genetic counseling session is recommended before testing
  • Sample can be blood, extracted DNA, or blood on FTA card
  • No fasting required for this test

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"This test is crucial for individuals with a family history of colon cancer or symptoms, enabling early intervention and tailored treatment strategies."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood, Extracted DNA, or One drop Blood on FTA Card
Collection MethodVenipuncture for blood sample or provided DNA sample

Sample Stability

Blood samples should be stored at ambient room temperature and processed within recommended timeframes
Sample Rejection Criteria:
  • Hemolyzed or contaminated samples
  • Insufficient sample volume

Understanding Your Results

Results indicate the presence or absence of pathogenic genetic mutations in the analyzed genes associated with colon cancer. Positive results may suggest increased risk or guide treatment, while negative results indicate no detected mutations in the panel.
📊

Positive for pathogenic variant

Increased risk of colon cancer; recommend genetic counseling, enhanced surveillance, and possible preventive measures.

📊

Negative for pathogenic variant

No mutations detected in the tested genes; however, risk may still exist due to other factors; follow standard screening guidelines.

📊

Variant of uncertain significance (VUS)

Genetic change found but clinical significance unknown; further testing and family studies may be needed.

⚠️ When to Consult a Doctor:

Consult a doctor if you experience symptoms of colon cancer, have a family history of the disease, or receive a positive test result for further evaluation and management.

Limitations

  • Test may not detect all genetic variants
  • Results require interpretation by a genetic counselor or healthcare provider

Risks & Considerations

  • Minor bruising or discomfort at the blood collection site
  • Minimal risk of infection from venipuncture

Interfering Factors

  • Sample contamination
  • Improper sample storage or handling

Frequently Asked Questions

What is the Colon Cancer Comprehensive Panel NGS Genetic Test?
It is a genetic test that uses next-generation sequencing to analyze multiple genes associated with colon cancer, helping to detect mutations for risk assessment and diagnosis.
Who should consider this test?
Individuals with a family history of colon cancer, symptoms such as changes in bowel habits or blood in stool, or those diagnosed with colon cancer for mutation analysis.
How is the test performed?
The test requires a blood sample, extracted DNA, or a blood drop on an FTA card, which is analyzed using NGS technology in a laboratory.
What is the cost of the test?
The cost is INR 35000, which includes home sample collection across India.
Is fasting required before the test?
No, fasting is not required for this genetic test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do the results mean?
Results indicate the presence or absence of genetic mutations; positive results may suggest increased risk, while negative results mean no mutations were detected in the tested genes.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings across many cities in India.
What genes are included in the panel?
The panel includes genes such as APC, ATM, BRCA1, BRCA2, MLH1, MSH2, and others linked to hereditary colon cancer syndromes.
Can this test diagnose colon cancer?
The test detects genetic mutations associated with colon cancer, which can aid in diagnosis when combined with clinical evaluation, but it is not a standalone diagnostic tool.
Is genetic counseling recommended?
Yes, a genetic counseling session is recommended before and after testing to understand results and implications.
What should I do if I receive a positive result?
Consult a healthcare provider or genetic counselor for further evaluation, surveillance recommendations, and possible preventive measures.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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LIMS Integration

Your Data Privacy

Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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