Sequence types and features ontology
340 terms(s) returned
| Term Type: | Record: 101 to 150 of 340 Records | Page: 3 of 7, First Previous Next Last | Show Records Per Page |
- sequence_alteration_artifact
- sequence_assembly
- sequence_attribute
- sequence_collection
- sequence_comparison
- sequence_conflict
- sequence_difference
- sequence_feature
- sequence_feature_locating_method
- sequence_length_alteration
- sequence_length_variant
- sequence_location
- sequence_motif
- sequence_of
- sequence_operation
- sequence_rearrangement_feature
- sequence_replication_mode
- sequence_secondary_structure
- sequence_source
- sequence_uncertainty
- sequence_variant
- sequence_variant_affecting_3D_structure_of_polypeptide
- sequence_variant_affecting_copy_number
- sequence_variant_affecting_editing
- sequence_variant_affecting_gene_structure
- sequence_variant_affecting_level_of_translational_product
- sequence_variant_affecting_polyadenylation
- sequence_variant_affecting_polypeptide_amino_acid_sequence
- sequence_variant_affecting_polypeptide_function
- sequence_variant_affecting_rate_of_transcription
- sequence_variant_affecting_regulatory_region
- sequence_variant_affecting_splice_acceptor
- sequence_variant_affecting_splice_donor
- sequence_variant_affecting_splicing
- sequence_variant_affecting_transcript_processing
- sequence_variant_affecting_transcript_secondary_structure
- sequence_variant_affecting_transcription
- sequence_variant_affecting_translational_product
- sequence_variant_causes_exon_loss
- sequence_variant_causes_intron_gain
- sequence_variant_causing_amino_acid_coding_codon_change_in_transcript
- sequence_variant_causing_amino_acid_deletion
- sequence_variant_causing_amino_acid_insertion
- sequence_variant_causing_amino_acid_substitution
- sequence_variant_causing_compensatory_transcript_secondary_structure_mutation
- sequence_variant_causing_complex_3D_structural_change
- sequence_variant_causing_complex_change_of_translational_product
- sequence_variant_causing_conformational_change
- sequence_variant_causing_conservative_amino_acid_substitution
- sequence_variant_causing_conservative_missense_codon_change_in_transcript
