Mutation Databases

Mutation databases are online resources that store information on variations in the genetic code of organisms. They provide critical information on the study of genetics, evolutionary biology, and biochemistry, and are used to inform research into the causes and treatments of diseases. Mutation databases play an important role in identifying and characterizing gene mutations, allowing for further study on the role of genetic variation in health and disease. With the explosion of genetic data from large-scale DNA sequencing projects, mutation databases have become increasingly valuable tools for discovering and understanding the genetic basis of human traits and diseases.

← Journal of Big Data 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