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  2. Point mutation - Wikipedia

    en.wikipedia.org/wiki/Point_mutation

    A point mutation is a genetic mutation where a single nucleotide base is changed, inserted or deleted from a DNA or RNA sequence of an organism's genome. [1] Point mutations have a variety of effects on the downstream protein product—consequences that are moderately predictable based upon the specifics of the mutation.

  3. Point accepted mutation - Wikipedia

    en.wikipedia.org/wiki/Point_accepted_mutation

    An example of point mutations at an amino acid site coding for lysine. The missense mutations may be classed as point accepted mutations if the mutated protein is not rejected by natural selection. A point accepted mutation — also known as a PAM — is the replacement of a single amino acid in the primary structure of a protein with another ...

  4. Nonsense mutation - Wikipedia

    en.wikipedia.org/wiki/Nonsense_mutation

    Missense mutations differ from nonsense mutations since they are point mutations that exhibit a single nucleotide change to cause substitution of a different amino acid. A nonsense mutation also differs from a nonstop mutation , which is a point mutation that removes a stop codon.

  5. Mutation - Wikipedia

    en.wikipedia.org/wiki/Mutation

    Point mutations are modifications of single base pairs of DNA or other small base pairs within a gene. A point mutation can be reversed by another point mutation, in which the nucleotide is changed back to its original state (true reversion) or by second-site reversion (a complementary mutation elsewhere that results in regained gene ...

  6. Single-nucleotide polymorphism - Wikipedia

    en.wikipedia.org/wiki/Single-nucleotide_polymorphism

    nonsense – point mutation in a sequence of DNA that results in a premature stop codon, or a nonsense codon in the transcribed mRNA, and in a truncated, incomplete, and usually nonfunctional protein product (e.g. Cystic fibrosis caused by the G542X mutation in the cystic fibrosis transmembrane conductance regulator gene). [21]

  7. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.

  8. Mutation rate - Wikipedia

    en.wikipedia.org/wiki/Mutation_rate

    Mutation rates are not constant and are not limited to a single type of mutation; there are many different types of mutations. Mutation rates are given for specific classes of mutations. Point mutations are a class of mutations which are changes to a single base. Missense, nonsense, and synonymous mutations are three subtypes of point mutations ...

  9. Transversion - Wikipedia

    en.wikipedia.org/wiki/Transversion

    Illustration of a transversion: each of the 8 nucleotide changes between a purine and a pyrimidine (in red). The 4 other changes are transitions (in blue).. Transversion, in molecular biology, refers to a point mutation in DNA in which a single (two ring) purine (A or G) is changed for a (one ring) pyrimidine (T or C), or vice versa. [1]