|
mobile_element_deletion
|
SO_0002066 |
|
|
CDS_supported_by_peptide_spectrum_match
|
SO_0002071 |
|
|
no_sequence_alteration
|
SO_0002073 |
|
|
intergenic_1kb_variant
|
SO_0002074 |
|
|
incomplete_transcript_3UTR_variant
|
SO_0002076 |
|
|
incomplete_transcript_5UTR_variant
|
SO_0002077 |
|
|
incomplete_transcript_intronic_variant
|
SO_0002078 |
|
|
interchromosomal_translocation
|
SO_0002060 |
|
|
intrachromosomal_translocation
|
SO_0002061 |
|
|
complex_chromosomal_rearrangement
|
SO_0002062 |
|
|
complex_structural_alteration
|
SO_0001784 |
|
|
Alu_insertion
|
SO_0002063 |
|
|
LINE1_insertion
|
SO_0002064 |
|
|
SVA_insertion
|
SO_0002065 |
|
|
HERV_deletion
|
SO_0002067 |
|
|
SVA_deletion
|
SO_0002068 |
|
|
LINE1_deletion
|
SO_0002069 |
|
|
constitutive_promoter
|
SO_0002050 |
|
|
inducible_promoter
|
SO_0002051 |
|
|
dominant_negative_variant
|
SO_0002052 |
|
