FB2024_03 , released June 25, 2024
FB2024_03 , released June 25, 2024
CV Term Report
Help Close All Open All
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 Extrernal Ontologies
SO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles
 MNV (all annotations which use CV term, excluding "NOT" statements)     234
Spanning Tree (Parents/Children)
Only view relationship: 
sequence_alteration__
biological_region____|
                     substitution
                      |__MNV  246 rec.
                          |__MNP
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a substitution
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "multiple nucleotide substitution" EXACT
    "multiple nucleotide variant" EXACT
Secondary IDs
hide External Crossreferences & Linkouts