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loading...| Preferred Name |
sequence_variant |
| Synonyms |
Jannovar:sequence_variant ANNOVAR:unknown sequence variant VAAST:sequence_variant |
| Definitions |
A sequence_variant is a non exact copy of a sequence_feature or genome exhibiting one or more sequence_alteration. |
| ID |
http://purl.obolibrary.org/obo/SO_0001060 |
| definition |
A sequence_variant is a non exact copy of a sequence_feature or genome exhibiting one or more sequence_alteration. |
| has_exact_synonym |
Jannovar:sequence_variant sequence variant VAAST:sequence_variant |
| has_obo_namespace |
sequence |
| has_related_synonym |
ANNOVAR:unknown |
| id |
SO:0001060 |
| label |
sequence_variant |
| notation |
SO:0001060 |
| prefLabel |
sequence_variant |
| subClassOf |
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| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/SO_0001060 | Human Disease Ontology / 人类疾病本体 | LOOM | |
| http://purl.obolibrary.org/obo/SO_0001060 | Human Disease Ontology / 人类疾病本体 | SAME_URI |