indelien
Indelien is a term used in genetics to describe an insertion or deletion of nucleotides in a DNA sequence. These small-scale mutations can occur in any part of the genome, including coding regions, regulatory elements, or intergenic regions. Indels can range in size from a single nucleotide to several thousand base pairs.
The functional consequences of indel mutations vary widely depending on their location and size. If an indel
Indels that are multiples of three nucleotides, or those occurring in non-coding regions, may have less severe
Indel mutations are a common source of genetic variation and play a role in evolution and the