: MeSH: INDEL Mutation

Genetic Phenomena > Genetic Variation > Mutation > INDEL Mutation

Genetic Phenomena > Mutagenesis > INDEL Mutation

INDEL Mutation

A mutation named with the blend of insertion and deletion. It refers to a length difference between two ALLELES where it is unknowable if the difference was originally caused by a SEQUENCE INSERTION or by a SEQUENCE DELETION. If the number of nucleotides in the insertion/deletion is not divisible by three, and it occurs in a protein coding region, it is also a FRAMESHIFT MUTATION.

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