Why would a mutation in a somatic cell of a multicellular organism not necessarily result in a detectable phenotype?

Price et al. [(1999). J. Bacteriol. 181:2358–2362] conducted a genetic study of the toxin transport protein (PA) of Bacillus anthracis, the bacterium that causes anthrax in humans. Within the 2294-nucleotide gene in 26 strains they identified five point mutations—two missense and three synonyms—among different isolates. Necropsy samples from an anthrax outbreak in 1979 revealed a novel missense mutation and five unique nucleotide changes among ten victims. The authors concluded that these data indicate little or no horizontal transfer between different B. anthracis strains.

Which types of nucleotide changes (missense or synonyms) cause amino acid changes?

Explain the following processes involving chromosome mutations and cancer development.

How the chromosome mutation producing Burkitt lymphoma generates the disease.

Explain the following processes involving chromosome mutations and cancer development.

How the chromosome mutation producing the Philadelphia chromosome leads to CML.

What are the differences between a synonymous mutation, a missense mutation, and a nonsense mutation?

Most mutations are thought to be deleterious. Why, then, is it reasonable to state that mutations are essential to the evolutionary process?

Why is a random mutation more likely to be deleterious than beneficial?

Most mutations in a diploid organism are recessive. Why?

The effect of base-pair substitution mutations on protein function varies widely from no detectable effect to the complete loss of protein function (null allele). Why do the functional consequences of base-pair substitution vary so widely?