Substitution Mutation

Substitution mutation is a type of genetic mutation where one of the nucleotides in a gene’s DNA sequence is replaced by another nucleotide. As a result of this single-nucleotide change, a genetic code is altered, resulting in a different gene product (protein) being created, potentially giving rise to a new trait in the organism. Such changes are significant as they may lead to various diseases and disorders, and they can also influence the development of traits and characteristics. Substitution mutations are being studied in order to understand how they can affect various diseases and disorders, and to improve the diagnosis, prognosis, and treatments of those affected. Additionally, researchers are also working to gain insight into how substitution mutations can be used to improve crop yield and animal production in the field of agriculture.

← Journal of DNA And RNA Research

Related Articles

15 article(s) found

Branch Retinal Vein Occlusion in Factor V Leiden Mutation

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

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

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

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

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Transmutation of Sweat Glands - Eccrine Porocarcinoma

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

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Genetic-Mathematical Modelling of Mutational Processes in a Population

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

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

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

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

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

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

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

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