Mutation, Missense
A mutation in which a codon is mutated to one directing the incorporation of a different amino acid. This substitution may result in an inactive or unstable product. (From A Dictionary of Genetics, King and Stansfield, 5th ed)
Year introduced: 1999
PubMed search builder options
Subheadings:
Tree Number(s): G05.365.590.650
MeSH Unique ID: D020125
Entry Terms:
- Missense Mutation
- Missense Mutations
- Mutations, Missense
Previous Indexing:
See Also: