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Concept information

Genetic Phenomena > Genetic Variation > Mutation > INDEL Mutation
Genetic Phenomena > Mutagenesis > INDEL Mutation

Terme préférentiel

INDEL Mutation  

Type

  • mesh:Descriptor

Définition

  • 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.

Concept générique

Synonyme(s)

  • Insertion-Deletion Mutation

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-Z69CL4G0-S

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RDF/XML TURTLE JSON-LD Date de création 09/07/2007, dernière modification le 17/06/2016