when the single base change results in a codon that specifies the same amino acid as the original codon
the correct answer is C. a substitution i know this cause i have this book to this question and point mutation is not one of the answer and i found the answer in the book -No its substituton you jack wagon your books wrong
Point Mutation- a type of gene mutation in which only a single nucleotide in a gene has been changed.
Mutations that occur at one single nitrogen base are referred to as a point mutation.
false, point mutation is the change in any single base within DNA at a given time.it occurs only once during a single mutation
translocation .. this is wrong.its a point mutation :)
point mutation
A mutation
There are 5 different disorders that result in galactosemia differentiated into three main types. The worst is the Classic form and there are over 180 different mutations associated with this form. The GALT gene is modified by substitution is these examples. The most common one in Caucasian is a single substitution of arginine for glutamine at position 188 on the protein. Another mutation that occurs almost exclusively in individuals of African decent is a single substitution of leucine for serine at position 135.
No single mutation is responsible for this disease. It just happens by abnormality in the red blood cells. It affects the hemoglobin.
the correct answer is C. a substitution i know this cause i have this book to this question and point mutation is not one of the answer and i found the answer in the book -No its substituton you jack wagon your books wrong
The type of mutation that causes a defect in the gene (causing sickle cell anaemia) is a substitution mutation.A single nucleotide substitution (A to T) in the β-globin gene causes the amino acid valine to replace glutamic acid. This changes the resulting protein, causing a haemoglobin with an abnormal shape to be created.
The specific type of mutation resulting from a mistake during DNA replication will depend on the nature of the mistake and the type of nucleotide substitution that occurred. Some possible types of mutations include point mutations (such as a substitution, insertion, or deletion of a single nucleotide), frameshift mutations, or silent mutations.
Yes but Mutation point 😂 A. Point Mutation
Point Mutation is the mutation that involves a single or few nucleotide. This type of mutation replaces a single nucleotide to another.
A mutation
At single point or a single base, many things can happen.If it is changed by any chance (mutation) it may cause deleterious effect (a disease like sickle cell anemia). Single point may act as a singnal for a protein to bind and activate a biochemical process. It also do act as a splicing signal.
Point Mutation- a type of gene mutation in which only a single nucleotide in a gene has been changed.