|
sequence_variant_causing_polypeptide_elongation
|
SO_1000099 |
|
|
benign_variant
|
SO_0001770 |
|
|
RR_tract
|
SO_0000435 |
|
|
sequence_variant_causing_conservative_amino_acid_substitution
|
SO_1000094 |
|
|
disease_associated_variant
|
SO_0001771 |
|
|
target_site_duplication
|
SO_0000434 |
|
|
sequence_variant_causing_amino_acid_substitution
|
SO_1000093 |
|
|
disease_causing_variant
|
SO_0001772 |
|
|
non_LTR_retrotransposon_polymeric_tract
|
SO_0000433 |
|
|
sequence_variant_causing_amino_acid_insertion
|
SO_1000096 |
|
|
lethal_variant
|
SO_0001773 |
|
|
U5_three_prime_LTR_region
|
SO_0000432 |
|
|
three_prime_LTR_component
|
SO_0000849 |
|
|
sequence_variant_causing_nonconservative_amino_acid_substitution
|
SO_1000095 |
|
|
unique_variant
|
SO_0001764 |
|
|
rare_variant
|
SO_0001765 |
|
|
polymorphic_variant
|
SO_0001766 |
|
|
common_variant
|
SO_0001767 |
|
|
fixed_variant
|
SO_0001768 |
|
|
U3_five_prime_LTR_region
|
SO_0000429 |
|
