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 |