The loss of genetic material.
deletion
A deletion mutation can be dominant or recessive, depending on the specific gene affected and the consequences of the deletion on the protein encoded by that gene. In general, the impact of a deletion mutation on an individual's phenotype will determine whether it is dominant or recessive.
deletion mutation
Yes
Replication
deletion
nonsense mutation, missense mutation, frameshift muation, deletion or addition mutation
Deletion Mutation causes DiGeorges Syndrome.
frameshift mutation: deletion
A point mutation is not a frameshift mutation. Point mutations involve changes in a single nucleotide base, while frameshift mutations involve the insertion or deletion of nucleotide bases, causing a shift in the reading frame of the genetic code.
A one base left out mutation is called a deletion mutation. This type of mutation involves the loss of one or more nucleotides from a DNA sequence, which can lead to a frameshift mutation if not in multiples of three.
An insertion/deletion event.