Frameshift ~
It is called a point mutation. Depending on where the bases are, as far as in the codon, some are not harmful.
A mutation
Huntington's disease is caused by a gene mutation, specifically in the HTT gene on chromosome 4.
Point Mutation- a type of gene mutation in which only a single nucleotide in a gene has been changed.
A change in a gene could involve a mutation that alters the DNA sequence, affecting the function of the protein it codes for. A change in a chromosome could involve alterations in the structure, number, or distribution of genetic material, leading to genetic disorders or diseases.
Frameshift ~
Frameshift
This is called an insertion mutation.Some repeats, such as the repeats in the Huntington's gene, can be repeated too many times and then you have the deleterious mutation in this gene.
A permanent change in the gene's DNA sequence. Gene mutations involving one or a few nuckeotides is called point mutation. If a nucleotide is added or deleted, the bases are still read in groups of three, but now those groupings are shifted for every codon that follows. This is called frameshift mutation. Your welcome. (:
Frame shift mutation occurs when a new codon in inserted. Point mutations occurs when one base, sometimes two, are inserted.
A mutation in a gene can happen by addition, deletion or substitution of base pairs. This means that the order of the bases will change- a new base may be added, a base may be lost, or one base may be substituted for another. The result of these mutations is that it causes the DNA to code for a different protein. If a mutation occurs in a sex cell, the mutation can be passed on to an offspring and affect the offspring's phenotype.
A mutation in a gene can happen by addition, deletion or substitution of base pairs. This means that the order of the bases will change- a new base may be added, a base may be lost, or one base may be substituted for another. The result of these mutations is that it causes the DNA to code for a different protein. If a mutation occurs in a sex cell, the mutation can be passed on to an offspring and affect the offspring's phenotype.
It is called a point mutation. Depending on where the bases are, as far as in the codon, some are not harmful.
i don't know and i just ask you
A mutation in the LCT gene, which is responsible for producing the lactase enzyme, results in lactose tolerance. This mutation allows individuals to continue producing lactase into adulthood, enabling them to digest lactose, the sugar found in dairy products.
false
A mutation in a gene involves a change in the sequence of DNA bases, which can occur through substitutions, insertions, or deletions. This alteration can affect the amino acid sequence of the protein encoded by the gene, potentially altering its structure and function. Depending on the nature of the mutation, it can lead to beneficial, neutral, or harmful effects on the organism. In some cases, mutations can also disrupt regulatory elements, affecting gene expression.