From another angle: beneficial and detrimental.
mutation brings about variation which is the basis of evolution and the two types of variation are heritable and non-heritable
This is because mutations occur in x chromosomes. The male, who has "xy" sex chromosomes, will have the mutation if it is present in the x chromosome. Females, there is a smaller chance because there are two "xx" chromosomes, which reduces the chance that the mutation will be present.
Generally, mutation.
The two types are Dna, and fossils
Without mutation there can be no evolution. Without evolution there can be no speciation.
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......
gene mutation, chromosomal abberations
nonsense mutation, missense mutation, frameshift muation, deletion or addition mutation
when there is a two way exchange of genetic portion between two non-homologus chromosomes, its called reciprocal mutation, its a type of translocation mutation
Two types of gene mutations are chromosomal and point mutation. Chromosomal mutation alters a cell's chromosomes, while point mutation replaces single-base pair nucleotides with other nucleotides found in RNA or DNA.
insertion and deletion
Only one or two nucleotides are changed in a certain mutation. This is an example of a(n)
Frameshift mutations and Point mutations. The difference between the two are that point mutations occur at a single point in the DNA sequence and frameshift mutations shift the "reading frame" of the genetic message.
Frameshift
The three types of mutations are substitution (where one base is replaced with another), insertion (where an extra base is added), and deletion (where a base is removed). These mutations can alter the DNA sequence and potentially change the resulting protein.
genes
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).