{"code":"C20629","name":"Silent Mutation","terminology":"ncit","version":"26.09d","conceptStatus":"DEFAULT","leaf":false,"active":true,"synonyms":[{"name":"Synonymous","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"caDSR"},{"name":"Synonymous Variant","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"GDC"},{"name":"Exon Synonymous Mutation","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Exonic Synonymous Mutation","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Mutation, Silent","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Silent Mutation","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Synonymous Mutation","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Synonymous Variant","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Silent Mutation","type":"Preferred_Name","typeCode":"P108"}],"definitions":[{"definition":"A point mutation occurring within the protein-coding region of a gene, and which codes for the same amino acid as expected.","code":"P97","type":"DEFINITION","source":"NCI"}],"properties":[{"code":"P322","type":"Contributing_Source","value":"GDC"},{"code":"P366","type":"Legacy Concept Name","value":"Silent_Mutation"},{"code":"P375","type":"Maps_To","value":"Synonymous Variant"},{"code":"P106","type":"Semantic_Type","value":"Cell or Molecular Dysfunction"},{"code":"P207","type":"UMLS_CUI","value":"C1519323"}]}