| General Information | |||
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| Term | exon_variant | ID (Ontology) | SO:0001791 (Sequence Ontology) |
| Definition | A sequence variant that changes exon sequence. | ||
| Also Known As | "ANNOVAR:exonic" ; "exon variant" ; "Jannovar:exon_variant" (for all, see Synonyms field below) | ||
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| SO.org | |||
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| 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
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No relevant statements available
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gene_variant |__transcript_variant |__exon_variant 15199 rec. |__coding_sequence_variant 15198 rec. | |__initiator_codon_variant(+) 26 rec. | |__protein_altering_variant(+) 15170 rec. | |__synonymous_variant(+) 31 rec. | |__terminator_codon_variant(+) 3 rec. |__non_coding_transcript_exon_variant |__UTR_variant 1 rec. |__3_prime_UTR_variant(+) 1 rec. |__5_prime_UTR_variant(+) |
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| Is a | transcript_variant | ||
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External Crossreferences & Linkouts
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| http://snpeff.sourceforge.net/SnpEff_manual.html | |||