What is another word for deletion mutation?
Pronunciation: [dɪlˈiːʃən mjuːtˈe͡ɪʃən] (IPA) 
A deletion mutation is a type of genetic mutation that involves the loss or removal of one or more nucleotides from the DNA sequence. This type of mutation can have significant consequences for the genetic information carried by the affected DNA, leading to the production of abnormal proteins and potentially causing genetic diseases. Synonyms for deletion mutation might include terms like frame-shift mutation, chromosomal deletion, gene deletion, or loss-of-function mutation, as all of these describe various aspects of the same basic genetic alteration. While deletion mutations can be harmful, they can also occasionally be beneficial, offering advantages such as increased resistance to diseases like HIV.
