{"code":"C164674","name":"Single Nucleotide Variant","terminology":"ncit","version":"26.09d","conceptStatus":"DEFAULT","leaf":true,"active":true,"synonyms":[{"name":"Single Nucleotide Variants","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"caDSR"},{"name":"SNV, NOS","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"caDSR"},{"name":"snv variant","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"CTDC"},{"name":"snv_variant","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"CTDC"},{"name":"Single-Nucleotide Variant","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"FDA","subSource":"pFDA"},{"name":"Single Nucleotide Variant","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"SNV","termType":"SY","type":"FULL_SYN","typeCode":"P90","source":"NCI"},{"name":"Single Nucleotide Variant","type":"Preferred_Name","typeCode":"P108"},{"name":"Single Nucleotide Variant","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"PCDC","subSource":"GCT"},{"name":"Single Nucleotide Variant","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"PCDC","subSource":"ALL"},{"name":"Single Nucleotide Variant","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"PCDC","subSource":"EWS"},{"name":"Single Nucleotide Variant","termType":"PT","type":"FULL_SYN","typeCode":"P90","source":"PCDC","subSource":"AML"}],"definitions":[{"definition":"A variation of a single nucleotide at a specific location of the genome due to base substitution, which is found at any frequency in the population.","code":"P97","type":"DEFINITION","source":"NCI"}],"properties":[{"code":"P322","type":"Contributing_Source","value":"CTDC"},{"code":"P322","type":"Contributing_Source","value":"FDA"},{"code":"P322","type":"Contributing_Source","value":"PCDC"},{"code":"P208","type":"NCI_META_CUI","value":"CL977820"},{"code":"P106","type":"Semantic_Type","value":"Nucleotide Sequence"}]}