deletion mutation from peptide sequence

Ontology CARD's Model Ontology
Accession MO:0000042
DefinitionA peptide sequence change between the translation initiation (start) and termination (stop) codon where, compared to a reference sequence, one or more amino acids are deleted and therefore are not present. These represent in-frame deletions which do not result in frameshift variants and may include multiple amino acids. Format is given by [wildtype AA][position]del for a single peptide deletion or [wildtype AA][position]_[wildtype AA][position]del for a deleted peptide range, e.g. K527del or Q517_N518del.
Classification3 ontology terms | Show
Parent Term(s)2 ontology terms | Show
Curator Acknowledgements
Curator Description Most Recent Edit