Biochemical Process

Mutation

AMW:PHYS:050329

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.

Physiology functional

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Mutation has parent Genetic Variation

DNA Repeat Expansion has parent Mutation

Base Pair Mismatch has parent Mutation

Gene Amplification has parent Mutation

Codon, Nonsense has parent Mutation

Allelic Imbalance has parent Mutation

Frameshift Mutation has parent Mutation

Gain of Function Mutation has parent Mutation

Gene Duplication has parent Mutation

Genomic Instability has parent Mutation

Germ-Line Mutation has parent Mutation

INDEL Mutation has parent Mutation

Loss of Function Mutation has parent Mutation

Mutation Accumulation has parent Mutation

Mutation, Missense has parent Mutation

Point Mutation has parent Mutation

Sequence Deletion has parent Mutation

Sequence Inversion has parent Mutation

Silent Mutation has parent Mutation

Suppression, Genetic has parent Mutation

Synthetic Lethal Mutations has parent Mutation

Mutagenesis, Insertional has parent Mutation

Mutation Rate has parent Mutation

Chromosome Aberrations has parent Mutation

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