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.
In the absence of ADP, the conversion of NADH to NAD+ via the electron transport chain is prevented from happening.
<h3>What is glycolysis?</h3>
Glycolysis is the series of reactions by which glucose is broken down to pyruvate by the body.
NAD+ is a limiting factor in glycolysis. In the absence of ADP, the conversion of NADH to NAD+ via the electron transport chain is prevented from happening.
In conclusion, NAD+ is a limiting factor in glycolysis.
Learn more about glycolysis at: brainly.com/question/4355201
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Answer:
There is a 25% percent chance that the child will have unattached earlobes, and a 50% percent chance that the child will have a widows peak.
Explanation: