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loading...| Preferred Name |
Insertion Mutation |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C19295 |
| code |
C19295 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C177537 |
| Contributing_Source |
CTRP GDC |
| DEFINITION |
Any rearrangement to the genomic content that adds one or more extra nucleotides into the DNA. Insertions may be reversible, particulary if caused by transposable elements. They may alter the reading frame of a gene, or may cause large scale additions of genomic DNA. |
| Display_Name |
Insertion Mutation |
| FULL_SYN |
Insertion Mutation Insertion Insertion NOS ins Insertion Mutation Abnormality |
| Is_Value_For_GDC_Property | |
| label |
Insertion Mutation |
| Legacy Concept Name |
Insertion_Mutation |
| Maps_To |
Insertion |
| Preferred_Name |
Insertion Mutation |
| prefixIRI |
Thesaurus:C19295 |
| prefLabel |
Insertion Mutation |
| Semantic_Type |
Cell or Molecular Dysfunction |
| UMLS_CUI |
C1512796 |
| subClassOf |
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