chromosomal mutation
This type of mutation is called a translocation mutation. It involves the movement of a segment of DNA from one chromosome to another non-homologous chromosome, leading to potential genetic changes and abnormalities.
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
translocation
This is a type of mutation called translocation.
A mutation in which a single base is added to or deleted from DNA is called an insertion or deletion mutation, also known as an indel mutation. This can lead to a shift in the reading frame during translation, causing significant changes in the resulting protein sequence and potentially leading to functional consequences.
A very small number.
translocation
Deletion, insertion, inversion, translocation, and duplication [for the ppl. Who dnt kno!!]
Hemophilia is a mutation of either of the genes that make factor VII or IX. Hemophilia A is a mutation of the F8 gene and Hemophilia B is the mutation of the F9 gene. Both of these mutations occur on the sex-linked X chromosome.
Color blindness is typically caused by a genetic mutation affecting the genes responsible for color vision, such as the OPN1LW and OPN1MW genes on the X chromosome. It is not usually associated with translocation or deletion of genetic material.
Translocation
Nondisjunction is a mutation where chromosomes fail to separate properly during cell division, leading to an abnormal number of chromosomes in daughter cells. Translocation is a mutation where a segment of one chromosome breaks off and attaches to another chromosome, potentially disrupting the normal genetic sequence.