Concept information
Preferred term
Mutation
Type
-
mesh:Descriptor
Definition
- Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations.
Broader concept
Narrower concepts
- Allelic Imbalance
- Base Pair Mismatch
- Chromosome Aberrations
- Codon, Nonsense
- DNA Repeat Expansion
- Frameshift Mutation
- Gain of Function Mutation
- Gene Amplification
- Gene Duplication
- Genomic Instability
- Germ-Line Mutation
- INDEL Mutation
- Loss of Function Mutation
- Mutagenesis, Insertional
- Mutation Accumulation
- Mutation, Missense
- Mutation Rate
- Point Mutation
- Sequence Deletion
- Sequence Inversion
- Silent Mutation
- Suppression, Genetic
- Synthetic Lethal Mutations
Allowable Qualifier(s)
In other languages
-
French
URI
http://data.loterre.fr/ark:/67375/JVR-Z5N478GX-B
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