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
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