[{"most_severe_consequence":"?","id":"COSM476","allele_string":"COSMIC_MUTATION","colocated_variants":[{"end":140453136,"phenotype_or_disease":1,"seq_region_name":"7","strand":1,"start":140453136,"allele_string":"HGMD_MUTATION","id":"CM112509"},{"phenotype_or_disease":1,"end":140453136,"somatic":1,"allele_string":"COSMIC_MUTATION","id":"COSM18443","strand":1,"start":140453136,"seq_region_name":"7"},{"phenotype_or_disease":1,"end":140453136,"somatic":1,"allele_string":"COSMIC_MUTATION","id":"COSM476","strand":1,"start":140453136,"seq_region_name":"7"},{"id":"COSM6137","allele_string":"COSMIC_MUTATION","seq_region_name":"7","start":140453136,"strand":1,"phenotype_or_disease":1,"somatic":1,"end":140453136}],"input":"COSM476","end":140453136,"assembly_name":"GRCh37","seq_region_name":"7","start":140453136,"strand":1}]