Before you know what a nucleotide substitution error is, you have to know what a nucleotide is. A nucleotide holds the DNA strand together and helps make copies. When a Strand is ready to be copied, Let's say one nucleotide reads for G(Guanine), then another nucleotide would be added, which would mean C (Cytosine) would be added. A substitution error would mean that, that instead of Cytosine being added, Thymine, Adenine, Uracil, or Guanine could be added, resulting in a mutation.
frameshift mutation
The substituted nucleotide has the same directions as the original nucleotide.
The substituted nucleotide has the same directions as the original nucleotide.
Point mutations
point mutation
Substitution
frameshift mutation
Base substitution is a type of mutation that involves the substitution of a nucleotide base. It may be categorized as a transition or transversion.
thymine....uracil is its substitution.
The substituted nucleotide has the same directions as the original nucleotide.
The substituted nucleotide has the same directions as the original nucleotide.
Point mutations
A substitution mutation in genetics is where one of the nucleotide bases of DNA is swapped for another. These mutations may or may not affect the protein that is being coded.
point mutation
true
the substitution has little effect because UGU and UGC both translate into the same amino acid--cysteine.
The types of point mutations are: base-pair substitution, insertions, deletions, and frameshift mutations. In base-pair substitution, one nucleotide and its corresponding partner are replaced with another pair of nucleotide. In insertion, nucleotide pairs are added to a gene. In deletion, nucleotide pairs are taken out of a gene. Frameshift mutation happens as a result of insertion or deletion when more or less than three (or a multiple of three) nucleotide pairs are added to or taken from a gene.