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so_table.tsv
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Civic SequenceOntology
3_prime_UTR_truncation SO_0002015
3_prime_UTR_variant SO_0001624
5_prime_UTR_exon_variant SO_0002092
5_prime_UTR_variant SO_0001623
amino_acid_deletion SO_0001604
coding_sequence_variant SO_0001580
coding_transcript_ SO_0001619
coding_transcript_variant SO_0002096
copy_number_change SO_0001563
disruptive_inframe_deletion SO_0001826
DNA_binding_site SO_0001429
dominant_negative_variant SO_0002052
exon_loss_variant SO_0001572
exon_variant SO_0001791
feature_truncation SO_0001906
frameshift_elongation SO_0001909
frameshift_truncation SO_0001910
frameshift_variant SO_0001589
gain_of_function_variant SO_0002053
gene_fusion SO_0001565
gene_silenced_by_DNA_methylation SO_0000129
gene_variant SO_0001564
inframe_deletion SO_0001822
inframe_indel SO_0001820
inframe_insertion SO_0001821
inframe_variant SO_0001650
insertion SO_0000667
intron_variant SO_0001627
loss_of_function_variant SO_0002054
loss_of_heterozygosity SO_0001786
microsatellite SO_0000289
minus_1_frameshift SO_0000866
minus_1_frameshift_variant SO_0001592
missense_variant SO_0001583
nonsynonymous_variant SO_0001992
plus_1_frameshift_variant SO_0001594
polymorphic_sequence_variant SO_0001025
protein_altering_variant SO_0001818
regulatory_region_variant SO_0001566
short_tandem_repeat_variation SO_0002096
silent_mutation SO_0001017
SNP SO_0000694
splice_acceptor_variant SO_0001574
splice_donor_variant SO_0001575
start_lost SO_0002012
stop_gained SO_0001587
stop_lost SO_0001578
synonymous_variant SO_0001819
transcript_ablation SO_0001893
transcript_amplification SO_0001889
transcript_fusion SO_0001886
transcript_regulatory_region_fusion SO_0001890
transcript_variant SO_0001576
transcription_variant SO_0001549
wild_type SO_0000817
coding_transcript_intron_variant SO_0001969
conservative_inframe_deletion SO_0001825
direct_tandem_duplication SO_1000039