| General Information | ||||||||
|---|---|---|---|---|---|---|---|---|
| Term | MNV | ID (Ontology) | SO:0002007 (Sequence Ontology) | |||||
| Definition | An MNV is a multiple nucleotide variant (substitution) in which the inserted sequence is the same length as the replaced sequence. | |||||||
| Also Known As | "multiple nucleotide substitution" ; "multiple nucleotide variant" | |||||||
| Comment | ||||||||
| Links to External Ontologies | ||||||||
| SO.org | ||||||||
| Annotations | ||||||||
| Records annotated with this term OR any of its CHILD TERMS | ||||||||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
||||||||
|
||||||||
|
||||||
sequence_alteration__ biological_region____| substitution |__MNV 315 rec. |__MNP |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | substitution | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||