[{"SO_term":"feature_truncation","label":"feature truncation","description":"A sequence variant that causes the reduction of a genomic feature, with regard to the reference sequence","SO_accession":"SO:0001906"},{"SO_accession":"SO:0001566","SO_term":"regulatory_region_variant","description":"A sequence variant located within a regulatory region","label":"regulatory region variant"},{"SO_accession":"SO:0001567","description":"A sequence variant where at least one base in the terminator codon is changed, but the terminator remains","label":"stop retained variant","SO_term":"stop_retained_variant"},{"SO_term":"feature_elongation","label":"feature elongation","description":"A sequence variant that causes the extension of a genomic feature, with regard to the reference sequence","SO_accession":"SO:0001907"},{"SO_accession":"SO:0001891","label":"regulatory region amplification","description":"A feature amplification of a region containing a regulatory region","SO_term":"regulatory_region_amplification"},{"label":"non coding transcript exon variant","description":"A sequence variant that changes non-coding exon sequence in a non-coding transcript","SO_term":"non_coding_transcript_exon_variant","SO_accession":"SO:0001792"},{"label":"coding sequence variant","description":"A sequence variant that changes the coding sequence","SO_term":"coding_sequence_variant","SO_accession":"SO:0001580"},{"label":"regulatory region ablation","description":"A feature ablation whereby the deleted region includes a regulatory region","SO_term":"regulatory_region_ablation","SO_accession":"SO:0001894"},{"SO_accession":"SO:0001623","SO_term":"5_prime_UTR_variant","description":"A UTR variant of the 5' UTR","label":"5 prime UTR variant"},{"SO_accession":"SO:0001587","label":"stop gained","description":"A sequence variant whereby at least one base of a codon is changed, resulting in a premature stop codon, leading to a shortened transcript","SO_term":"stop_gained"},{"label":"downstream gene variant","description":"A sequence variant located 3' of a gene","SO_term":"downstream_gene_variant","SO_accession":"SO:0001632"},{"SO_accession":"SO:0002012","SO_term":"start_lost","label":"start lost","description":"A codon variant that changes at least one base of the canonical start codon"},{"SO_accession":"SO:0001620","SO_term":"mature_miRNA_variant","label":"mature miRNA variant","description":"A transcript variant located with the sequence of the mature miRNA"},{"SO_accession":"SO:0001968","SO_term":"coding_transcript_variant","label":"coding transcript variant","description":"A transcript variant of a protein coding gene"},{"SO_term":"intron_variant","description":"A transcript variant occurring within an intron","label":"intron variant","SO_accession":"SO:0001627"},{"SO_accession":"SO:0001578","SO_term":"stop_lost","description":"A sequence variant where at least one base of the terminator codon (stop) is changed, resulting in an elongated transcript","label":"stop lost"},{"SO_term":"frameshift_variant","description":"A sequence variant which causes a disruption of the translational reading frame, because the number of nucleotides inserted or deleted is not a multiple of three","label":"frameshift variant","SO_accession":"SO:0001589"},{"SO_accession":"SO:0001631","description":"A sequence variant located 5' of a gene","label":"upstream gene variant","SO_term":"upstream_gene_variant"},{"label":"splice donor region variant","description":"A sequence variant that falls in the region between the 3rd and 6th base after splice junction (5' end of intron).","SO_term":"splice_donor_region_variant","SO_accession":"SO:0002170"},{"SO_term":"splice_donor_5th_base_variant","description":"A sequence variant that causes a change at the 5th base pair after the start of the intron in the orientation of the transcript","label":"splice donor 5th base variant","SO_accession":"SO:0001787"},{"SO_accession":"SO:0001619","SO_term":"non_coding_transcript_variant","label":"non coding transcript variant","description":"A transcript variant of a non coding RNA gene"},{"SO_accession":"SO:0001819","SO_term":"synonymous_variant","description":"A sequence variant where there is no resulting change to the encoded amino acid","label":"synonymous variant"},{"SO_accession":"SO:0001818","SO_term":"protein_altering_variant","label":"protein altering variant","description":"A sequence_variant which is predicted to change the protein encoded in the coding sequence"},{"SO_accession":"SO:0002019","SO_term":"start_retained_variant","label":"start retained variant","description":"A sequence variant where at least one base in the start codon is changed, but the start remains"},{"SO_term":"sequence_variant","description":"A sequence_variant is a non exact copy of a sequence_feature or genome exhibiting one or more sequence_alteration","label":"sequence variant","SO_accession":"SO:0001060"},{"SO_accession":"SO:0001782","description":"A sequence variant located within a transcription factor binding site","label":"TF binding site","SO_term":"TF_binding_site_variant"},{"SO_term":"transcript_ablation","label":"transcript ablation","description":"A feature ablation whereby the deleted region includes a transcript feature","SO_accession":"SO:0001893"},{"SO_accession":"SO:0001583","description":"A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preserved","label":"missense variant","SO_term":"missense_variant"},{"SO_accession":"SO:0002169","SO_term":"splice_polypyrimidine_tract_variant","label":"splice polypyrimidine tract variant","description":"A sequence variant that falls in the polypyrimidine tract at 3' end of intron between 17 and 3 bases from the end (acceptor -3 to acceptor -17)"},{"SO_accession":"SO:0001624","SO_term":"3_prime_UTR_variant","label":"3 prime UTR variant","description":"A UTR variant of the 3' UTR"},{"description":"An inframe non synonymous variant that inserts bases into in the coding sequence","label":"inframe insertion","SO_term":"inframe_insertion","SO_accession":"SO:0001821"},{"SO_term":"TFBS_ablation","description":"A feature ablation whereby the deleted region includes a transcription factor binding site","label":"TFBS ablation","SO_accession":"SO:0001895"},{"SO_term":"splice_donor_variant","label":"splice donor variant","description":"A splice variant that changes the 2 base region at the 5' end of an intron","SO_accession":"SO:0001575"},{"SO_accession":"SO:0001892","description":"A feature amplification of a region containing a transcription factor binding site","label":"TFBS amplification","SO_term":"TFBS_amplification"},{"label":"splice region variant","description":"A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intron","SO_term":"splice_region_variant","SO_accession":"SO:0001630"},{"SO_accession":"SO:0001621","description":"A variant in a transcript that is the target of NMD","label":"NMD transcript variant","SO_term":"NMD_transcript_variant"},{"SO_accession":"SO:0001574","SO_term":"splice_acceptor_variant","description":"A splice variant that changes the 2 base region at the 3' end of an intron","label":"splice acceptor variant"},{"SO_accession":"SO:0001626","SO_term":"incomplete_terminal_codon_variant","description":"A sequence variant where at least one base of the final codon of an incompletely annotated transcript is changed","label":"incomplete terminal codon variant"},{"SO_term":"transcript_amplification","description":"A feature amplification of a region containing a transcript","label":"transcript amplification","SO_accession":"SO:0001889"},{"SO_accession":"SO:0001628","description":"A sequence variant located in the intergenic region, between genes","label":"intergenic variant","SO_term":"intergenic_variant"},{"description":"An inframe non synonymous variant that deletes bases from the coding sequence","label":"inframe deletion","SO_term":"inframe_deletion","SO_accession":"SO:0001822"}]