insertion mutation from nucleotide sequence

Accession MO:0000045
DefinitionA subtype of the insertion mutation detection model parameter. This parameter is used when a set of insertion mutations is reported in a nucleotide sequence format. Such mutations may be of variable length - possibly causing a frameshift, but not causing premature termination or a functional knockout. Mutation parameters of this type are reported in CARD with the notation: [+]nt[position]:[nucleotides].
Classification3 ontology terms | Show
Parent Term(s)3 ontology terms | Show