Silent Mutation

A silent mutation is a type of genetic mutation that results in no observable change in the protein product made from a gene. These mutations occur due to changes in the sequence of DNA that are not reflected in the amino acid sequence of the protein. They are thought to be important in the evolution of species because they can be inherited without introducing any detrimental effects. Silent mutations can also affect how a gene is expressed, leading to changes in physiology and behavior. In addition, since silent mutations do not cause any changes in the protein product, they can also affect the regulation of gene expression and the effectiveness of gene therapy treatments.

← Journal of DNA And RNA Research

Related Articles

15 article(s) found

Branch Retinal Vein Occlusion in Factor V Leiden Mutation

Full-text HTML Download PDF Download XML

Skeletal Muscle Calcium Channel Mutation R528G: Enhanced Channel Inactivation and Omega-Current at Hyperpolarization Contribute to Hypokalemic Periodic Paralysis.

Full-text HTML Download PDF Download XML

The Identification of Somatic Mutations in Interferon-G Signal Molecules in Human Uterine Leiomyosarcoma

Full-text HTML Download PDF Download XML

Recurrent branch retinal arterial occlusions associated with plasminogen activator inhibitor-1 mutation

Full-text HTML Download PDF Download XML

Melanoma of the Breast with Smoothened (SMO) Mutation: Case Report and review of the Literature

Full-text HTML Download PDF Download XML

Transmutation of Sweat Glands - Eccrine Porocarcinoma

Full-text HTML Download PDF Download XML

Characterization of rpoB Gene Mutations Associated with Rifampicin Resistance in Multidrug Resistant Tuberculosis Patients Co-infected with HIV from Southern India.

Full-text HTML Download PDF Download XML

Genetic-Mathematical Modelling of Mutational Processes in a Population

Full-text HTML Download PDF Download XML

An Algorithm to Predict the Possible SARS-CoV-2 Mutations

Full-text HTML Download PDF Download XML

A New Gene Mutation of PRKAR1A was found in a Carney Complex Case

Full-text HTML Download PDF Download XML

Targeting Mutational Landscape of TP53 in patients diagnosed with Oral Cancer living in Senegal

Full-text HTML Download PDF Download XML

Prolonged survival of Diamond-Blackfan anemia and RPS19 mutation: an observation in Togo

Full-text HTML Download PDF Download XML

A Trio Study Showing Novel Gene Mutation In LAMB3 Causing Junctional Epidermolysis Bullosa (Intermediate/ Severe)

Full-text HTML Download PDF Download XML

Understanding Inherited Bleeding Disorders: Genetic Mutations in Blood Coagulation Factors and Regulatory Proteins

Full-text HTML Download PDF Download XML

Disruption of Hydrogen Bonding Network Decreases Catalytic Diversity of Chloroperoxidase via Abolishing Both Chlorination and Dismutation Activities

Full-text HTML Download PDF Download XML