An Inversion mutation is a mutation that causes a reversal in the order of a segment of a chromosome within the chromosome, or a gene.
mutations
Four types of chromosomal mutations are Down syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).
A mutation is the term for any permanent change in a gene or chromosome. Mutations can be caused by various factors, such as errors during DNA replication or exposure to certain environmental factors like radiation or chemicals.
Mutation
Four types of chromosomal mutations are Down syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).
Translocations
mutation
Mutation
Polyploidy
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.
it is a mutation of the gene FRG3 in chromosome 4