chromosomal mutation

Noun
  1. (genetics) any event that changes genetic structure;
    Any alteration in the inherited nucleic acid sequence of the genotype of an organism (synset 107439611)
    referred to in: genetic science, genetics - the branch of biology that studies heredity and variation in organisms
    is a type of: alteration, change, modification - an event that occurs when something passes from one state or phase to another
    subtypes:
    • deletion - (genetics) the loss or absence of one or more nucleotides from a chromosome
    • inversion - (genetics) a kind of mutation in which the order of the genes in a section of a chromosome is reversed
    • transposition - (genetics) a kind of mutation in which a chromosomal segment is transfered to a new position on the same or another chromosome
    • gene mutation, point mutation - (genetics) a mutation due to an intramolecular reorganization of a gene
    • reversion - (genetics) a return to a normal phenotype (usually resulting from a second mutation)
    • saltation - (genetics) a mutation that drastically changes the phenotype of an organism or species
    has: mutagenesis - an event capable of causing a mutation
    same as: genetic mutation, mutation

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