{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":26,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:11892","source":"HGNC:11892|tumor necrosis factor","targets":["1048804|NC_000006.12:g.31575324G>A|single nucleotide variant|Uncertain significance|TNF|no assertion criteria provided|6","12385|L29S|Variation|Pathogenic|TNF|no assertion criteria provided|","12386|NM_000594.4(TNF):c.322C>T (p.Arg108Trp)|single nucleotide variant|Pathogenic|TNF|no assertion criteria provided|6","12387|NC_000006.12:g.31575186G>A|single nucleotide variant|risk factor|TNF|no assertion criteria provided|6","12389|NC_000006.12:g.31574705C>T|single nucleotide variant|risk factor|TNF|no assertion criteria provided|6","12390|NC_000006.12:g.31574699C>A|single nucleotide variant|protective|TNF|no assertion criteria provided|6","1697317|NM_000594.4(TNF):c.17T>A (p.Met6Lys)|single nucleotide variant|Uncertain significance|TNF|criteria provided, single submitter|6","225964|NC_000006.12:g.31575254G>A|single nucleotide variant|drug response|TNF|reviewed by expert panel|6","2301391|NM_000594.4(TNF):c.121G>T (p.Val41Leu)|single nucleotide variant|Uncertain significance|TNF|criteria provided, single submitter|6","2480132|NM_000594.4(TNF):c.350T>C (p.Val117Ala)|single nucleotide variant|Uncertain significance|TNF|criteria provided, single submitter|6","3180153|NM_000594.4(TNF):c.320G>T (p.Arg107Leu)|single nucleotide variant|Uncertain significance|TNF|criteria provided, single submitter|6","3327449|NM_000594.4(TNF):c.550G>C (p.Gly184Arg)|single nucleotide variant|Uncertain significance|TNF|criteria provided, single submitter|6","3362893|TNF, 20-BP INS, NT190|Insertion|Pathogenic|TNF|no assertion criteria provided|","3892678|NM_000594.4(TNF):c.248C>A (p.Thr83Asn)|single nucleotide variant|Uncertain significance|TNF|criteria provided, single submitter|6","4277959|NM_000594.4(TNF):c.161G>A (p.Gly54Glu)|single nucleotide variant|Uncertain significance|TNF|criteria provided, single submitter|6","4325540|NM_000594.4(TNF):c.186+74G>T|single nucleotide variant||TNF||6","4325541|NM_000594.4(TNF):c.187-3C>G|single nucleotide variant||TNF||6","4325542|NM_000594.4(TNF):c.280+1G>C|single nucleotide variant||TNF||6","4597303|NM_000594.4(TNF):c.169G>A (p.Gly57Ser)|single nucleotide variant|Uncertain significance|TNF|criteria provided, single submitter|6","4597304|NM_000594.4(TNF):c.196G>A (p.Asp66Asn)|single nucleotide variant|Uncertain significance|TNF|criteria provided, single submitter|6","723481|NM_000594.4(TNF):c.477C>T (p.Ile159=)|single nucleotide variant|Likely benign|TNF|criteria provided, single submitter|6","732409|NM_000594.4(TNF):c.489C>T (p.Tyr163=)|single nucleotide variant|Likely benign|TNF|criteria provided, single submitter|6","748239|NM_000594.4(TNF):c.354G>A (p.Glu118=)|single nucleotide variant|Likely benign|TNF|criteria provided, single submitter|6","761640|NM_000594.4(TNF):c.39C>A (p.Ala13=)|single nucleotide variant|Likely benign|TNF|criteria provided, single submitter|6","781865|NM_000594.4(TNF):c.251C>T (p.Pro84Leu)|single nucleotide variant|Benign/Likely benign|TNF|criteria provided, multiple submitters, no conflicts|6","784495|NM_000594.4(TNF):c.87G>T (p.Arg29=)|single nucleotide variant|Benign|TNF|criteria provided, single submitter|6"]}]}