deletion mutation from nucleotide sequence

Accession MO:0000043
DefinitionA subtype of the deletion mutation detection model parameter. This parameter is used when a set of deletion mutations is reported in a nucleotide sequence format. Such mutations may be of variable length - possibly causing a frameshift, but not premature termination of functional knockout. Mutation parameters of this type are reported in the CARD with the notation: [-]nt[position]:[nucleotides].
Classification3 ontology terms | Show
Parent Term(s)3 ontology terms | Show