Concept information
Término preferido
INDEL Mutation
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Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- Insertion-Deletion Mutation
En otras lenguas
-
francés
-
Mutation INDEL
-
Mutation par insertion-délétion
URI
http://data.loterre.fr/ark:/67375/JVR-Z69CL4G0-S
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