FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
CV Term Report
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General Information
Term inframe_insertion ID (Ontology) SO:0001821 (Sequence Ontology)
Definition An inframe non synonymous variant that inserts bases into in the coding sequence.
Also Known As "ANNOVAR:nonframeshift insertion" ; "inframe increase in CDS length" ; "inframe insertion" (for all, see Synonyms field below)
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SO.org
Annotations
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 Alleles
 inframe_insertion (all annotations which use CV term, excluding "NOT" statements)      38
Spanning Tree (Parents/Children)
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inframe_variant
 |__inframe_indel________________
feature_elongation               |
 |__internal_feature_elongation__|
                                 inframe_insertion  39 rec.
                                  |__conservative_inframe_insertion
                                  |__disruptive_inframe_insertion 1 rec.
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Is a inframe_indel
internal_feature_elongation
Part of
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Synonyms
  • "ANNOVAR:nonframeshift insertion" EXACT VAR
    "inframe codon gain" RELATED
    "inframe increase in CDS length" EXACT
    "inframe insertion" EXACT
    "inframe_codon_gain" EXACT
    "Jannovar:inframe_insertion" EXACT VAR
    "snpEFF:CODON_INSERTION" EXACT VAR
    "VAT:insertionNFS" EXACT VAR
    "VEP:inframe_insertion" EXACT VAR
Secondary IDs
hide External Crossreferences & Linkouts
http://snpeff.sourceforge.net/SnpEff_manual.html
http://vat.gersteinlab.org/formats.php "VAT"
http:www.ensembl.org/info/genome/variation/predicted_data.html#consequences