{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":41,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:5992","source":"HGNC:5992|interleukin 1 beta","targets":["1049443|NM_000576.3(IL1B):c.28G>A (p.Glu10Lys)|single nucleotide variant|Uncertain significance|IL1B|no assertion criteria provided|2","120093|NM_000576.3(IL1B):c.99+383G>C|single nucleotide variant|not provided|IL1B|no classification provided|2","14671|NC_000002.12:g.112836810G>A|single nucleotide variant|risk factor|IL1B|no assertion criteria provided|2","2210683|NM_000576.3(IL1B):c.145C>A (p.Gln49Lys)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","2258916|NM_000576.3(IL1B):c.114C>A (p.Asp38Glu)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","2260904|NM_000576.3(IL1B):c.92A>G (p.Gln31Arg)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","2267927|NM_000576.3(IL1B):c.303A>T (p.Glu101Asp)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","2392768|NM_000576.3(IL1B):c.562G>A (p.Val188Met)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","2520520|NM_000576.3(IL1B):c.160G>A (p.Asp54Asn)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","2533024|NM_000576.3(IL1B):c.238C>T (p.Pro80Ser)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","2651287|NM_000576.3(IL1B):c.309C>A (p.Ile103=)|single nucleotide variant|Likely benign|IL1B|criteria provided, single submitter|2","3050880|NM_000576.3(IL1B):c.100-5C>T|single nucleotide variant|Likely benign|IL1B|no assertion criteria provided|2","3109228|NM_000576.3(IL1B):c.364C>G (p.Leu122Val)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","3109229|NM_000576.3(IL1B):c.423A>C (p.Glu141Asp)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","3109230|NM_000576.3(IL1B):c.668A>G (p.Asn223Ser)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","4274892|NM_000576.3(IL1B):c.214G>A (p.Asp72Asn)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","4274893|NM_000576.3(IL1B):c.43T>C (p.Tyr15His)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","4274894|NM_000576.3(IL1B):c.419A>G (p.Tyr140Cys)|single nucleotide variant|Likely benign|IL1B|criteria provided, single submitter|2","4502968|NM_000576.3(IL1B):c.*375A>T|single nucleotide variant||IL1B||2","4502969|NM_000576.3(IL1B):c.*358A>T|single nucleotide variant||IL1B||2","4502971|NM_000576.3(IL1B):c.*354A>T|single nucleotide variant||IL1B||2","4502972|NM_000576.3(IL1B):c.597+5G>C|single nucleotide variant||IL1B||2","4502973|NM_000576.3(IL1B):c.597+1G>A|single nucleotide variant||IL1B||2","4502974|NM_000576.3(IL1B):c.561C>T (p.Cys187=)|single nucleotide variant||IL1B||2","4502975|NM_000576.3(IL1B):c.495A>T (p.Gly165=)|single nucleotide variant||IL1B||2","4502976|NM_000576.3(IL1B):c.491A>T (p.Gln164Leu)|single nucleotide variant||IL1B||2","4502977|NM_000576.3(IL1B):c.466+182A>G|single nucleotide variant||IL1B||2","4502978|NM_000576.3(IL1B):c.315C>A (p.Phe105Leu)|single nucleotide variant||IL1B||2","4502979|NM_000576.3(IL1B):c.302-3C>T|single nucleotide variant||IL1B||2","4502983|NM_000576.3(IL1B):c.301+6T>C|single nucleotide variant||IL1B||2","4502984|NM_000576.3(IL1B):c.193G>A (p.Ala65Thr)|single nucleotide variant||IL1B||2","4502987|NM_000576.3(IL1B):c.47G>T (p.Ser16Ile)|single nucleotide variant||IL1B||2","4502989|NM_000576.3(IL1B):c.-16+188G>T|single nucleotide variant||IL1B||2","4678545|NM_000576.3(IL1B):c.704A>G (p.Asn235Ser)|single nucleotide variant|Uncertain significance|IL1B|criteria provided, single submitter|2","772847|NM_000576.3(IL1B):c.100-10C>T|single nucleotide variant|Benign|IL1B|criteria provided, multiple submitters, no conflicts|2","779077|NM_000576.3(IL1B):c.171C>T (p.Tyr57=)|single nucleotide variant|Benign/Likely benign|IL1B|criteria provided, multiple submitters, no conflicts|2","780097|NM_000576.3(IL1B):c.138C>T (p.Gly46=)|single nucleotide variant|Benign|IL1B|criteria provided, multiple submitters, no conflicts|2","869137|NM_000576.3(IL1B):c.315C>T (p.Phe105=)|single nucleotide variant|Benign; Affects; association; other|IL1B|no assertion criteria provided|2","869138|NC_000002.12:g.112837290A>G|single nucleotide variant|association|IL1B|no assertion criteria provided|2","869139|NC_000002.12:g.112838252C>G|single nucleotide variant|association|IL1B|no assertion criteria provided|2","916339|NM_000576.3(IL1B):c.630G>A (p.Lys210=)|single nucleotide variant|Likely benign|IL1B|criteria provided, single submitter|2"]}]}