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Its deletion duplicating inversion and translational
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Which types of mutation can add genes to a chromosomes?
insertion and deletion
Describe four types of mutation resulting from the breakage of chromosome?
Deletion: a segment of the chromosome is lost during breakage. Duplication: a segment of the chromosome is copied and inserted back into the chromosome following breakage. Inversion: a segment of the chromosome is reversed and re-inserted following breakage. Translocation: a segment of the chromosome breaks off and joins a different chromosome.
What kind of mutation will result from the mistake made during DNA replication in the nucleotide sequence above?
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.
Which types of mutation causes sickle cell anemia?
Sickle cell anemia is caused by a point mutation in the HBB gene, specifically a substitution of adenine for thymine in the sixth codon of the gene, resulting in the production of abnormal hemoglobin known as hemoglobin S.
What are 3 types of mutations and what do they do?
The three different types of mutation are substitution, insertion, and deletion. They differ because deletion is missing a base, insertion has a base that was added, and substitution has a base that has been replaced.
Describe four types of mutations resulting from the breakage of chromosomes?
Deletion, duplication, inversion, translocation.
Which types of mutation can add genes to a chromosomes?
insertion and deletion
Describe four types of mutation resulting from the breakage of chromosome?
Deletion: a segment of the chromosome is lost during breakage. Duplication: a segment of the chromosome is copied and inserted back into the chromosome following breakage. Inversion: a segment of the chromosome is reversed and re-inserted following breakage. Translocation: a segment of the chromosome breaks off and joins a different chromosome.
What is the 2 types of breakage?
The two types of breakage are physical breakage, which involves the actual splitting or fracturing of an object, and emotional breakage, which refers to the psychological or emotional damage or distress experienced by an individual.
List two types of gene mutations?
Point mutations: involve a change in a single nucleotide within the DNA sequence, leading to the substitution of one base for another. Frameshift mutations: occur when nucleotides are either deleted or inserted into the DNA sequence, causing a shift in the reading frame and potentially altering the entire sequence downstream.
Name 2 major types of mutation?
i] spontaneous mutation ii] induced mutation iii] germinal mutation iv] somatic mutation v] chromosomal mutation vi] gene mutation are the some of the major types of mutation......
Which of the following types of mutation resulting in an error in the mRNA just after the AUG start of translation is likely to have the most serious effect on the polypeptide product?
A frameshift mutation, such as an insertion or deletion of a nucleotide, that occurs just after the AUG start codon is likely to have the most serious effect on the polypeptide product. This is because frameshift mutations shift the reading frame of the mRNA sequence, causing all subsequent codons to be read incorrectly, leading to a completely altered polypeptide sequence.
What are the major types of mutation event?
gene mutation, chromosomal abberations
What are the types of mutations that can occur?
nonsense mutation, missense mutation, frameshift muation, deletion or addition mutation
What types of cells are seen in chromosomes?
Cells are not found in chromosomes. Chromosomes are found in cells.
What are two types of mutation?
From another angle: beneficial and detrimental.
What is a karyotype and what type of mutation does it show?
A karyotype is a visual representation of an individual's chromosomes. It can show various types of mutations, such as deletions, duplications, translocations, and inversions, by displaying changes in the number or structure of chromosomes.
