insertion mutation from nucleotide sequence

Accession MO:0000045
DefinitionA subtype of the insertion mutation detection model parameter used when a set of insertion mutations are reported in a nucleotide sequence format, encoded as [+]nt[position]:[nucleotides], for example +nt391:GG or +nt368:18. Such mutations may be of variable length, possibly causing a frameshift but not causing premature termination or a functional knockout.
Classification3 ontology terms | Show
Parent Term(s)3 ontology terms | Show
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