mutation
Articles
- ClastogenSubstance that can cause breaks in chromosomes
- HeteroplasmyPolymorphism of organellar DNA sequences in a cell
- C957T
- Frameshift mutationMutation that shifts codon alignment
- Resistance mutation (virology)Virus mutation
- Insertion (genetics)Type of mutation
- Fusion geneGene formed by the combination of two independent genes
- Fusion geneGene formed by the combination of two independent genes
- Sherman paradoxEarly term for the triplet-repeat pattern of inheritance found in fragile X syndrome
- HomoplasmyIdentity of organellar DNA sequences in a cell
- Mutation–selection balanceAllele equilibrium in a population when creation equals elimination by negative selection
- TransversionDNA point mutation that exchanges a purine (A or G) for a pyrimidine (C or T) or vice versa
- Fusion geneGene formed by the combination of two independent genes
- HeteroplasmyPolymorphism of organellar DNA sequences in a cell
- HomoplasmyIdentity of organellar DNA sequences in a cell
- Fusion geneGene formed by the combination of two independent genes
- Fusion geneGene formed by the combination of two independent genes
- HeteroplasmyPolymorphism of organellar DNA sequences in a cell
- HomoplasmyIdentity of organellar DNA sequences in a cell
- GenotoxicityConcept in toxicology
- Sequence feature variant typeMutation of a given sequence feature in a protein
- Splice site mutationMutation at a location where intron splicing takes place
- Micronucleus testTest for potential genotoxic compounds
- BRCA mutation
- Obligate carrier