What are 3 things that a substitution mutation cause?
Three Things That A Substitution Mutation Can CauseChange in the coding of amino acids codon to a particular stop codon resulting in an incomplete protein, which is usually non-functional.Can cause Silent mutations where a codon change can encode the same amino acid resulting in no changes in the protein synthesized.More items….
What does a substitution mutation cause?
A substitution is a mutation that exchanges one base for another (i.e., a change in a single “chemical letter” such as switching an A to a G). Such a substitution could: change a codon to one that encodes a different amino acid and cause a small change in the protein produced.
What diseases are caused by point mutations?
Contents4.1 Cancer.4.2 Neurofibromatosis.4.3 Sickle-cell anemia.4.4 Tay–Sachs disease.4.5 Color blindness.
What are the 4 types of mutation?
There are three types of DNA Mutations: base substitutions, deletions and insertions.Base Substitutions. Single base substitutions are called point mutations, recall the point mutation Glu —–> Val which causes sickle-cell disease.Deletions. … Insertions.
Is substitution mutation harmful?
Because an insertion or deletion results in a frame-shift that changes the reading of subsequent codons and, therefore, alters the entire amino acid sequence that follows the mutation, insertions and deletions are usually more harmful than a substitution in which only a single amino acid is altered.
What are the causes of mutation?
These changes can be caused by environmental factors such as ultraviolet radiation from the sun, or can occur if an error is made as DNA copies itself during cell division. Acquired mutations in somatic cells (cells other than sperm and egg cells) cannot be passed to the next generation.