Genetic sequencing analysis of full protein-coding gene mutations in whole blood
This test involves analyzing your blood sample to identify specific genetic mutations across all protein-coding genes. It helps detect variations that may influence your health, including risks for inherited conditions.
["This test helps identify genetic mutations that could affect your risk for certain diseases or conditions."]
Key facts at a glance
- LOINC
- 92994-3
- Short code
- PROS1 gene Full Mut Anl Bld/T Seq
- Synonyms
- PROS1 gene Full Mut Anl Bld/T Seq
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- sequencing
- 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 examines DNA sequences from your whole blood to identify any mutations in the genes responsible for producing proteins. These mutations can be inherited or may arise spontaneously. The focus is on full-length protein-coding regions, ensuring comprehensive coverage of potential genetic variations.
How the Test Works
Your blood sample is processed to extract DNA. Advanced sequencing technology reads the genetic code, comparing it against a reference database to pinpoint any mutations. The results highlight specific gene changes that may require further medical evaluation.
Preparation and Sample Collection
No special preparation is needed for this test. A simple blood draw is performed by a healthcare professional. The sample is then sent to a laboratory for genetic sequencing analysis, which can take several days to complete.
Clinical Significance
Genetic mutations detected by this test may indicate an increased risk for inherited disorders, such as metabolic diseases, cancer predispositions, or neurological conditions. Early identification can guide preventive measures, monitoring, or tailored treatment plans.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Genetic sequencing results are used to assess risks for inherited conditions, inform personalized healthcare decisions, and support genetic counseling. Results should always be interpreted by a healthcare provider familiar with your medical history and family genetics.
Frequently asked questions
Why might I need this test?
What does a positive result mean?
How long will I need to wait for results?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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