Genetic mutation analysis for *RPS6KA3* (RSK3) via next-generation sequencing
This test checks for specific changes (mutations) in the RPS6KA3 gene, which may be linked to certain genetic conditions or cancer risks. It uses blood drawn from you to analyze DNA.
["This test helps identify inherited or acquired genetic variations that could affect health."]
Key facts at a glance
- LOINC
- 53793-6
- Short code
- RPS6KA3 gene Mut Anl tier1 Bld/T
- Synonyms
- RPS6KA3 gene Mut Anl tier1 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
Why This Test Might Be Ordered
Your healthcare provider may recommend this test if you have a family history of certain cancers (like breast, ovarian, or prostate), developmental disorders, or if symptoms suggest a genetic condition. It could also be part of a broader genetic screening or diagnostic workup.
What to Expect Before the Test
No special preparation is needed. You’ll have a small needle inserted into your arm to draw a blood sample. The process takes about 5 minutes, and you may feel slight discomfort. If you’re pregnant or have a bleeding disorder, let your provider know before the test.
What Happens During the Test
Your blood sample is sent to a lab where it’s processed to extract DNA. Specialized equipment reads the genetic code to detect any mutations in the RPS6KA3 gene. Results are analyzed by trained professionals to determine if mutations are present.
What the Results Mean
Results will be reported as either *positive* (mutation detected) or *negative* (no mutation found). If a mutation is found, it may indicate an increased risk for certain conditions or guide further testing or treatment options. Results are discussed with your healthcare provider to interpret their clinical relevance.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Clinical Significance
Short name
RPS6KA3 Mutation Test
Frequently asked questions
How long will I get my results?
What if my test is positive for a mutation?
Can I get this test if I don’t have a family history of genetic conditions?
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