Its deletion duplicating inversion and translational
insertion and deletion
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.
The child would inherit one set of chromosomes from each parent. Since the male is homozygous for the normal gene order, he will pass on a normal chromosome set. The female, being homozygous for the inversion mutation, will pass on chromosomes that carry the inversion. As a result, the child will have one set of normal chromosomes and one set with the inversion mutation, leading to a genotype that is heterozygous for the inversion.
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.
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.
Deletion, duplication, inversion, translocation.
insertion and deletion
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.
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......
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.
a gene is passed on from generations and a chromosome is just found in certain cells
The child would inherit one set of chromosomes from each parent. Since the male is homozygous for the normal gene order, he will pass on a normal chromosome set. The female, being homozygous for the inversion mutation, will pass on chromosomes that carry the inversion. As a result, the child will have one set of normal chromosomes and one set with the inversion mutation, leading to a genotype that is heterozygous for the inversion.
gene mutation, chromosomal abberations
nonsense mutation, missense mutation, frameshift muation, deletion or addition mutation
Cells are not found in chromosomes. Chromosomes are found in cells.
From another angle: beneficial and detrimental.
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.