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Kitexon® 8-Mutant Load Blood Test (Genetic Mutation Analysis)

Published: August 9, 2026Updated: August 16, 2026

This test measures the combined genetic load of 8 specific mutations in your blood, often used to assess inherited risks for certain genetic conditions.

Quick summary

["Helps identify genetic predispositions that may require further evaluation or monitoring."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
87733-2
Short code
KIT Exon 8 Mut Anl Bld/T
Synonyms
KIT Exon 8 Mut Anl Bld/T
Category
chemistry
Sample
whole-blood
Container
Lavender-top (EDTA)
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Method
molgen
Specimen volume
3 mL
Stability
Room temperature: 4h, Refrigerated: 24h
Hemolysis max
0
Lipemia max
0
Icterus max
0
TAT
4–24 hours
Order
routine

What This Test Measures

The test detects the presence and quantity of 8 distinct genetic mutations across your blood sample. These mutations may be associated with conditions like certain cancers, metabolic disorders, or other hereditary diseases. The results are expressed as a 'mutant load,' which reflects the proportion of mutated genetic material compared to normal DNA.

Why It Might Be Ordered

Your healthcare provider may recommend this test if you have a family history of genetic disorders, are at increased risk for certain cancers, or if you’re part of a genetic screening program. It’s also used in research or clinical trials focused on hereditary conditions.

Sample Collection and Preparation

A small blood sample is drawn from a vein, typically in your arm. The sample is processed to isolate DNA, which is then analyzed for the 8 specified mutations. No special preparation is needed before the test, but fasting may be required depending on the clinical context.

Test Results Interpretation

Results are presented as a 'mutant load percentage,' showing how many of your cells carry the mutations. A higher load may indicate an increased risk for associated conditions, but results alone do not diagnose a specific disease. Interpretation depends on clinical context, family history, and genetic counseling.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

◆Associated findings1

Short name

8-Mutant Load Test

Frequently asked questions

How might this test affect my care?
If your results show a high mutant load, your healthcare provider may recommend additional genetic testing, lifestyle adjustments, or monitoring for potential symptoms. Some mutations may guide preventive strategies, such as regular screenings or early interventions. Always discuss results with your provider to understand their implications for your health.
What does a positive result mean?
A positive result means you carry the mutations being tested, but it doesn’t confirm a diagnosis. It may suggest an increased risk for certain conditions, prompting further evaluation. Your provider will consider your family history, symptoms, and other test results to guide next steps.
Can this test be used for screening in children?
Yes, this test can be used in children if there’s a family history of the associated genetic conditions. Genetic counselors can help explain the risks and benefits of testing, especially for younger patients. Always consult your healthcare provider before proceeding.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy