A mutation is a permanent alteration in the DNA sequence that makes up a gene, resulting in a variant form.
A mutation occurs only due to environmental factors.
A mutation is a temporary change in the DNA sequence.
Mutations always result in lethal genetic disorders.
The main types of mutations include point mutations, insertions, deletions, and chromosomal mutations.
Point mutations and amino acid changes.
Insertions, deletions, and silent mutations only.
Only point mutations and inversions.
A point mutation is a genetic mutation that involves a change of a single nucleotide base in the DNA sequence.
A point mutation involves multiple chromosome changes.
It is when DNA replication errors affect entire genes.
A type of chromosomal mutation affecting DNA.
Mutations can occur spontaneously due to errors during DNA replication or induced by environmental factors such as radiation and chemicals.
Spontaneous mutations cannot happen without chemical exposure.
They only occur during extreme genetic experiments.
Mutations occur spontaneously due to poor nutrition.
A silent mutation is a type of mutation where the change in nucleotide does not result in a different amino acid and thus does not alter the protein function.
Silent mutations greatly alter protein function.
It causes new nutrient requirements.
A silent mutation results in a complete gene change.
A frameshift mutation occurs when nucleotides are inserted or deleted from the DNA sequence, causing a shift in the reading frame of the genetic code.
It is a mutation only affecting chromosome numbers.
Frameshift mutations repair DNA sequence errors.
It involves exchanging entire DNA sequences.