World Of Taxonomy
C171175Level 6

Delins Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in a nucleotide sequence where nucleotides in a reference sequence are replaced by other nucleotides and which is not a substitution, inversion or conversion.

**Synonyms:** - Deletion-Insertion - Deletion-Insertion - Deletion-Insertion Variant - delins - delins Variant - delins variant - delins_variant

GET/api/v1/systems/nci_thesaurus/nodes/C171175
Official DownloadCC BY 4.0Source

Hierarchy Explorer

Loading...

Cross-system equivalences0

No cross-system equivalences mapped for this node.