Genetic Full Mutation Analysis of Blood DNA (Targeted Sequencing)
This test analyzes specific genetic mutations in your blood DNA to identify variations in targeted genes that may be associated with certain inherited conditions.
["Helps detect known genetic changes linked to specific health risks or conditions."]
Key facts at a glance
- LOINC
- 94235-9
- Short code
- F7 gene Full Mut Anl Bld/T Seq
- Synonyms
- F7 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
This test involves sequencing DNA extracted from your blood sample to identify full mutations (deletions, duplications, or substitutions) in a predefined set of genes. The results focus on detecting specific genetic variants that may be clinically relevant, such as those linked to hereditary disorders or cancer predispositions.
How the Test Works
Your blood sample is processed to isolate DNA. Advanced sequencing technology reads the genetic code to compare your DNA against a reference sequence for the targeted genes. The test may also assess copy number variations (CNVs) or structural rearrangements in the genes of interest.
Why It Might Be Ordered
A healthcare provider may recommend this test if you have a family history of genetic disorders, symptoms suggestive of a genetic condition, or if you are at higher risk for certain cancers or other inherited conditions. It can also be used for prenatal screening, carrier testing, or as part of a diagnostic workup.
Sample Collection and Preparation
A blood sample is drawn from a vein in your arm. The blood is processed to extract DNA, which is then prepared for sequencing. This process typically takes a few days to complete before results are available.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Short name
N/A
Frequently asked questions
Genetic mutations detected by this test can indicate an increased risk for inherited conditions, guide personalized treatment plans, or inform decisions about family planning. Identifying these mutations helps healthcare providers tailor management strategies to your specific genetic profile.
What does a positive result mean?
How long will it take to get 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