[{"seq_region_name":"7","most_severe_consequence":"?","end":140753336,"colocated_variants":[{"allele_string":"HGMD_MUTATION","start":140753336,"strand":1,"id":"CM112509","seq_region_name":"7","phenotype_or_disease":1,"end":140753336},{"allele_string":"COSMIC_MUTATION","strand":1,"id":"COSV56056643","start":140753336,"somatic":1,"end":140753336,"phenotype_or_disease":1,"seq_region_name":"7","var_synonyms":{"COSMIC":["COSM476"]}},{"start":140753336,"strand":1,"id":"COSV56065204","allele_string":"COSMIC_MUTATION","var_synonyms":{"COSMIC":["COSM18443"]},"seq_region_name":"7","phenotype_or_disease":1,"end":140753336,"somatic":1},{"id":"COSV56080151","strand":1,"start":140753336,"allele_string":"COSMIC_MUTATION","var_synonyms":{"COSMIC":["COSM6137"]},"somatic":1,"seq_region_name":"7","phenotype_or_disease":1,"end":140753336}],"allele_string":"COSMIC_MUTATION","assembly_name":"GRCh38","input":"COSM476","start":140753336,"strand":1,"id":"COSM476"}]