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loading...| Preferred Name |
Silent Mutation |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C20629 |
| code |
C20629 |
| Concept_In_Subset | |
| Contributing_Source |
GDC |
| DEFINITION |
A point mutation occurring within the protein-coding region of a gene, and which codes for the same amino acid as expected. |
| FULL_SYN |
Exon Synonymous Mutation Exonic Synonymous Mutation Mutation, Silent Silent Mutation Synonymous Mutation Synonymous Synonymous Variant |
| Is_Value_For_GDC_Property | |
| label |
Silent Mutation |
| Legacy Concept Name |
Silent_Mutation |
| Maps_To |
Synonymous Variant |
| Preferred_Name |
Silent Mutation |
| prefixIRI |
Thesaurus:C20629 |
| prefLabel |
Silent Mutation |
| Semantic_Type |
Cell or Molecular Dysfunction |
| UMLS_CUI |
C1519323 |
| subClassOf |
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