| Descriptor English: | Point Mutation | ||||
| Descriptor Spanish: |
Mutación Puntual
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| Descriptor Portuguese: | Mutação Puntual | ||||
| Descriptor French: | Mutation ponctuelle | ||||
| Entry term(s): |
Mutation, Point Mutations, Point Point Mutations |
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| Tree number(s): |
G05.365.590.675 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D017354 | ||||
| Scope note: | A mutation caused by the substitution of one nucleotide for another. This results in the DNA molecule having a change in a single base pair. |
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| Annotation: | see MUTATION for correct use of /drug eff & /rad eff |
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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: |
Mutation (1966-1992) |
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| Public MeSH Note: | 93 |
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| History Note: | 93 |
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| Related: |
Mutation, Missense
MeSH | ||||
| DeCS ID: | 30613 | ||||
| Unique ID: | D017354 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 1993/01/01 | ||||
| Date of Entry: | 1992/05/22 | ||||
| Revision Date: | 2008/07/08 |
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PHENOMENA AND PROCESSES
Genetic Phenomena [G05]Genetic Phenomena
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Point Mutation
- Preferred
| Concept UI |
M0026348 |
| Scope note | A mutation caused by the substitution of one nucleotide for another. This results in the DNA molecule having a change in a single base pair. |
| Preferred term | Point Mutation |
| Entry term(s) |
Mutation, Point Mutations, Point Point Mutations |
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