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Mutation - Wikipedia
Mutations may or may not produce detectable changes in the observable characteristics ( phenotype) of an organism. Mutations play a part in both normal and abnormal biological processes including: evolution, cancer, and the development of the immune system, including junctional diversity.
Mutations (article) | Khan Academy
A mutation is any change to the nucleotide sequence of a DNA molecule. Some mutations arise as DNA is copied. Others are due to environmental factors. A mutation in a gene can change the structure and function of the protein encoded by that gene. This, in turn, can affect an organism’s traits.
Mutation
A mutation is a change in the DNA sequence of an organism. Mutations can result from errors in DNA replication during cell division, exposure to mutagens or a viral infection. Germline mutations (that occur in eggs and sperm) can be passed on to offspring, while somatic mutations (that occur in body cells) are not passed on.
Mutation - Definition, Types, Examples and Quiz - Biology Dictionary
Mutation Definition. At the simplest level, a mutation is a change or transformation. In biology, mutations refer to changes in chromosomes and genes, which typically manifest physically. The effect of a mutation can depend on the region in which the sequence of genetic material has been changed.
Mutation
A mutation is a change in the structure of a gene, the unit of heredity. Genes are made of deoxyribonucleic acid (DNA), a long molecule composed of building blocks called nucleotides.Each . nucleotide is built around one of four different subunits called bases.. These bases are known as guanine, cytosine, adenine, and thymine. A gene carries information in the sequence of its nucleotides, just ...
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