National Cancer Institute Thesaurus

Last uploaded: February 21, 2019

Preferred Name	Silent Mutation
ID	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C20629
code	C20629
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 Mutation, Silent Exonic Synonymous Mutation Synonymous Mutation
label	Silent Mutation
Legacy_Concept_Name	Silent_Mutation
Preferred_Name	Silent Mutation
prefixIRI	C20629
prefLabel	Silent Mutation
Semantic_Type	Cell or Molecular Dysfunction
UMLS_CUI	C1519323
subClassOf	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C62200

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/SO_0001017	Sequence Types and Features Ontology	LOOM
http://purl.obolibrary.org/obo/SO_0001017	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/MESH/D000069456	Medical Subject Headings	LOOM