CGG
GAA
A missense mutation is the change in a single nucleotide that results in a different amino acid being coded for. GCA codes for the amino acid Alanine.
Therefore any of the following changes would be missense mutations:
GAA -> Glutamic acid
GUA -> Valine
GGA -> Glycine
CCA -> Proline
UCA -> Serine
ACA -> Threonine
A missense mutation is the change in a single nucleotide that results in a different amino acid being coded for. GCA codes for the amino acid Alanine.
Therefore any of the following changes would be missense mutations:
GAA -> Glutamic acid
GUA -> Valine
GGA -> Glycine
CCA -> Proline
UCA -> Serine
ACA -> Threonine
cgg
Answer is GAA
The DNA sequence of gene that change AACTTG to AACATG are called missense mutation. This is known as a process.
A point mutation causes a change in the amino acid sequence creating a new type of protein. The mutations are categorized functionally as nonsense, missense and silent mutations.
A Missense Mutation.It is a point mutation where the mutations alters the base sequence without changing the resulting function of the subsequent protein. This is usually when the mutation does not change the amino acid which the codon codes for.
Any change in the sequence of DNA nucleotides is called mutation.
the permanent change is called mutation
The DNA sequence of gene that change AACTTG to AACATG are called missense mutation. This is known as a process.
Both a silent and missense mutation is a change in one nucleotide. However, a silent mutation still codes for the same amino acid, but a missense mutation codes for a different amino acid. This means that a silent mutation will have no affect on the resulting protein, but a missense mutation will. Still, it is not guaranteed that a a missense mutation will result in a disfunction of created protein, as long as it is not occurring in the activation site.
A point mutation causes a change in the amino acid sequence creating a new type of protein. The mutations are categorized functionally as nonsense, missense and silent mutations.
A Missense Mutation.It is a point mutation where the mutations alters the base sequence without changing the resulting function of the subsequent protein. This is usually when the mutation does not change the amino acid which the codon codes for.
Any change in the sequence of DNA nucleotides is called mutation.
The change is a mutation.
A change in the nucleotide sequence of DNA is called a mutation.
A change in the nucleotide sequence of DNA is called a mutation.
the permanent change is called mutation
a change in the DNA sequence is a mutation, so I'm not sure what you're asking
The change in the order of the bases in a DNA molecule is called a mutation. Such changes may happen because of damage to genomes, replication errors, or insertion or deletion of nucleotide bases.
mutation is a permanent change in the DNA sequence of a gene and can alter the amino acid sequence of the protein encoded by the gene..