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NUDT15 Gene Mutation Analysis Test

DNA Labs India | ISO 9001:2015 Certified

NUDT15 Gene Mutation Analysis Test

Short Name: NUDT15 Mutation Test

Also known as: NUDT15 Genotyping, Thiopurine Sensitivity Test

NUDT15 Gene Mutation Analysis Test test available at DNA Labs India for ₹7,500. Uses Sanger Sequencing on Peripheral blood samples. Results in Reports are typically available within 12 days after sample collection.. Free home collection in 300+ cities across India.

Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of NUDT15 gene mutation analysis is to identify genetic variants that predispose individuals to thiopurine drug toxicity. This information helps in personalizing treatment plans, adjusting drug doses, or avoiding thiopurines altogether to prevent serious side effects such as bone marrow suppression and infections.

Test Code
3132
Price
₹7,500
Sample Type
Peripheral blood
Result Time
Reports are typically available within 12 days after sample collection.
Fasting Required
No
Method
Sanger Sequencing
Step 1

Sample Collection

No specific preparation is required. Ensure a doctor's prescription is available if needed, though it may not be required for certain cases like surgery or pregnancy.

Method: Venipuncture

Step 2

Laboratory Analysis

A healthcare professional will collect a peripheral blood sample via venipuncture from a vein in the arm.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Resume normal activities unless otherwise advised.

Timeline: Reports are typically available within 12 days after sample collection.

Patient Instructions

1
Before the Test:No fasting required. Ensure a doctor's prescription is available if needed for insurance or procedural purposes.
2
During the Test:A blood sample will be drawn from your arm. The process takes about 5-10 minutes.
3
After the Test:You may resume normal activities immediately. Apply a bandage to the puncture site if needed.

About This Test

Who Should Get This Test

The purpose of NUDT15 gene mutation analysis is to identify genetic variants that predispose individuals to thiopurine drug toxicity. This information helps in personalizing treatment plans, adjusting drug doses, or avoiding thiopurines altogether to prevent serious side effects such as bone marrow suppression and infections.

How to Prepare

  • Bring a valid ID and doctor's prescription if applicable
  • Wear loose clothing to facilitate blood draw
  • Inform the phlebotomist of any bleeding disorders or medications

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"This test is essential for patients on thiopurine drugs to prevent severe side effects like bone marrow suppression. Genetic testing enables personalized dosing and safer treatment."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypePeripheral blood
Sample Volume2 ml
ContainerEDTA Vacutainer
Collection MethodVenipuncture

Sample Stability

Stable for 24 hours at room temperature (15-25°C)
For longer storage, refrigerate at 2-8°C for up to 7 days
Sample Rejection Criteria:
  • Insufficient sample volume
  • Contaminated or hemolyzed samples
  • Incorrect sample labeling

Understanding Your Results

Results indicate the presence or absence of NUDT15 gene mutations. A positive result suggests increased risk of thiopurine toxicity, while a negative result indicates lower risk, though other factors may still influence drug response.
📊

Negative (No Mutation)

No pathogenic NUDT15 variants detected. Standard thiopurine dosing may be considered, but clinical monitoring is still advised.

Action: Consult with your doctor for personalized treatment planning.

📊

Positive (Mutation Detected)

Pathogenic NUDT15 variant identified, indicating higher risk of thiopurine-induced toxicity.

Action: Discuss dose adjustment or alternative therapies with your healthcare provider. Genetic counseling may be recommended.

⚠️ When to Consult a Doctor:

Consult your doctor if you experience symptoms like nausea, vomiting, fever, fatigue, or jaundice while on thiopurine drugs, or before starting such therapy if you have a family history of toxicity.

Limitations

  • This test does not detect all possible genetic variants in the NUDT15 gene
  • Results should be interpreted in conjunction with clinical history and other tests
  • May not predict the severity of toxicity in all cases

Risks & Considerations

  • Minor bruising or pain at the blood draw site
  • Rare risk of infection or excessive bleeding
  • No significant long-term risks associated with the test

Interfering Factors

  • Hemolyzed or lipemic blood samples may affect test accuracy
  • Recent blood transfusions could interfere with genetic analysis
  • Improper sample storage or handling

Compare With Similar Tests

TestNUDT15 Gene Mutation AnalysisTPMT Gene Mutation AnalysisPharmacogenomic Panel
ComparisonNUDT15 Gene Mutation AnalysisBoth tests assess thiopurine drug metabolism, but NUDT15 focuses on a different gene linked to toxicity in Asian populations.A broader test that includes multiple genes affecting drug response, whereas NUDT15 analysis is specific to thiopurine toxicity.

Frequently Asked Questions

What is NUDT15 gene mutation analysis?
It is a genetic test that detects mutations in the NUDT15 gene, which can increase the risk of side effects from thiopurine drugs like azathioprine and 6-mercaptopurine.
Why is this test important?
It helps identify individuals at risk of severe thiopurine toxicity, allowing doctors to personalize drug dosages or choose alternative treatments to prevent adverse reactions.
Who should consider getting this test?
Individuals with a family history of thiopurine toxicity, those who have had adverse reactions to thiopurine drugs, or patients about to start thiopurine therapy for conditions like inflammatory bowel disease or leukemia.
How is the test performed?
It involves a simple blood draw. The sample is sent to a lab where DNA is analyzed using Sanger sequencing to detect NUDT15 mutations.
What is the cost of the test?
The test costs INR 7500 at DNA Labs India, which includes home sample collection in many cities across India.
Is fasting required before the test?
No, fasting is not required. You can eat and drink normally before the blood draw.
How long does it take to get results?
Results are typically available within 12 days after sample collection. You can access them online, via email, or WhatsApp.
What do the results mean?
A negative result means no pathogenic mutations were detected, indicating lower risk. A positive result means a mutation was found, suggesting higher risk of thiopurine toxicity, and your doctor may adjust treatment.
Are there any risks associated with the test?
The test involves minimal risks, such as slight bruising or pain at the blood draw site. Serious complications are rare.
Can this test be done at home?
Yes, DNA Labs India offers free home sample collection for this test in numerous cities across India. You can book online for convenience.
Is a doctor's prescription needed?
A doctor's prescription may be required for the test, but it is not applicable in cases of surgery, pregnancy, or for individuals planning to travel abroad.
How accurate is the test?
The test uses Sanger sequencing, which is highly accurate for detecting known NUDT15 mutations. However, it may not detect all rare variants, and results should be interpreted by a healthcare professional.
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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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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