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Extranuclear mutations are genetic changes that occur outside of the cell nucleus, typically in the mitochondria. These mutations can affect mitochondrial function and lead to various disorders, including mitochondrial diseases. Extracellular mutations can be inherited maternally and can have implications for energy production and cellular metabolism.
Two are insertion mutations and deletion mutations.
No, Mutations can not be predicted and have no numeral order. Mutations are totally random AND MAY NOT BE PREDICTED!
Examples of mutations include point mutations (substitution, insertion, deletion), chromosomal mutations (duplication, deletion, inversion, translocation), and silent mutations. These mutations can lead to various consequences such as changes in protein structure and function, genetic disorders, and cancer.
The three main types of gene mutations are point mutations, insertion mutations, and deletion mutations. Point mutations involve changes to a single nucleotide base. Insertion mutations involve the addition of extra nucleotide bases. Deletion mutations involve the removal of nucleotide bases in a gene sequence.
Gametic mutations occur in the cells of the gonads (which produce sperm and eggs) and may be inherited. There are two types of mutations that can occur in gamete cells: 1. Gene Mutations 2. Chromosomal Mutations