Answer:
A single nucleotide changes in CCG which will result in missense mutation can be many possibilities.
Explanation:
Missense mutations
CCG codes for Proline amino acid
• Mutation in first nucleotide codes for
UCG specifically encodes Serine
ACG specifically encodes Threonine
GCG specifically encodes Alanine
Missense mutation
• Mutation in second nucleotide specify for coding
CUG specifically encodes Leucine
CAG specifically encodes Glutamine
CGG specifically encodes Arginine
• Mutation in Third Nucleotide will not result in missense mutation because any point mutation in third nucleotide of codon will encode same amino acid i.e Proline.
