{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":7,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:6893","source":"HGNC:6893|microtubule associated protein tau","targets":["2049744|NM_001377265.1(MAPT):c.2091+16C>G|single nucleotide variant|Likely pathogenic|MAPT|criteria provided, single submitter|17","3075676|NM_001377265.1(MAPT):c.2077C>G (p.Pro693Ala)|single nucleotide variant|Likely pathogenic|MAPT|criteria provided, single submitter|17","3778831|NM_001377265.1(MAPT):c.2027T>A (p.Leu676His)|single nucleotide variant|Likely pathogenic|MAPT|criteria provided, single submitter|17","4056341|NM_001377265.1(MAPT):c.2010TAA[1] (p.Asn671del)|Microsatellite|Likely pathogenic|MAPT|criteria provided, single submitter|17","599620|NM_001377265.1(MAPT):c.2260C>T (p.His754Tyr)|single nucleotide variant|Likely pathogenic|MAPT|criteria provided, single submitter|17","807628|NM_001377265.1(MAPT):c.2266C>A (p.Pro756Thr)|single nucleotide variant|Likely pathogenic|MAPT|criteria provided, single submitter|17","986870|NM_001377265.1(MAPT):c.2242T>A (p.Ser748Thr)|single nucleotide variant|Likely pathogenic|MAPT|criteria provided, single submitter|17"]}]}