Descriptor English: | Mutation, Missense | ||||
Descriptor Spanish: |
Mutación Missense
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Descriptor Portuguese: | Mutação de Sentido Incorreto | ||||
Descriptor French: | Mutation faux-sens | ||||
Entry term(s): |
Missense Mutation Missense Mutations Mutations, Missense |
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Tree number(s): |
G05.365.590.650 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D020125 | ||||
Scope note: | 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 & Stansfield, 5th ed) |
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Allowable Qualifiers: |
DE drug effects ES ethics GE genetics IM immunology PH physiology RE radiation effects |
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Previous Indexing: |
Amino Acid Sequence (1966-1998) |
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Public MeSH Note: | 99 |
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History Note: | 99 |
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Related: |
Amino Acid Substitution
MeSH Point Mutation MeSH | ||||
DeCS ID: | 33909 | ||||
Unique ID: | D020125 | ||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
Date Established: | 1999/01/01 | ||||
Date of Entry: | 1998/06/10 | ||||
Revision Date: | 2008/07/08 |
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PHENOMENA AND PROCESSES
Genetic Phenomena [G05]Genetic Phenomena
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Mutation, Missense
- Preferred
Concept UI |
M0029865 |
Scope note | 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 & Stansfield, 5th ed) |
Preferred term | Mutation, Missense |
Entry term(s) |
Missense Mutation Missense Mutations Mutations, Missense |
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