{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":30,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:4010","source":"HGNC:4010|FUS RNA binding protein","targets":["1073222|NM_004960.4(FUS):c.1554_1557del (p.Gln519fs)|Microsatellite|Pathogenic|FUS|criteria provided, multiple submitters, no conflicts|16","1423819|NM_004960.4(FUS):c.1500dup (p.Gly501fs)|Duplication|Pathogenic|FUS|criteria provided, single submitter|16","1458206|NM_004960.4(FUS):c.1509_1510del (p.Gly504fs)|Microsatellite|Pathogenic|FUS|criteria provided, multiple submitters, no conflicts|16","1485282|NM_004960.4(FUS):c.1391_1392dup (p.Gly465fs)|Duplication|Pathogenic|FUS|criteria provided, single submitter|16","16221|NM_004960.4(FUS):c.1551C>G (p.His517Gln)|single nucleotide variant|Pathogenic|FUS|no assertion criteria provided|16","16222|NM_004960.4(FUS):c.1561C>G (p.Arg521Gly)|single nucleotide variant|Pathogenic|FUS|criteria provided, multiple submitters, no conflicts|16","16223|NM_004960.4(FUS):c.1553G>A (p.Arg518Lys)|single nucleotide variant|Pathogenic|FUS|criteria provided, single submitter|16","16224|NM_004960.4(FUS):c.1561C>T (p.Arg521Cys)|single nucleotide variant|Pathogenic|FUS|criteria provided, multiple submitters, no conflicts|16","16225|NM_004960.4(FUS):c.1562G>A (p.Arg521His)|single nucleotide variant|Pathogenic|FUS|criteria provided, multiple submitters, no conflicts|16","1918103|NM_004960.4(FUS):c.253C>T (p.Gln85Ter)|single nucleotide variant|Pathogenic|FUS|criteria provided, single submitter|16","2046744|NM_004960.4(FUS):c.1573C>A (p.Pro525Thr)|single nucleotide variant|Pathogenic|FUS|criteria provided, single submitter|16","2419096|NM_004960.4(FUS):c.1449_1488del (p.Tyr484fs)|Deletion|Pathogenic|FUS|criteria provided, single submitter|16","280109|NM_004960.4(FUS):c.1572G>C (p.Arg524Ser)|single nucleotide variant|Pathogenic|FUS|criteria provided, single submitter|16","280110|NM_004960.4(FUS):c.1574C>T (p.Pro525Leu)|single nucleotide variant|Pathogenic|FUS|criteria provided, multiple submitters, no conflicts|16","280356|NM_004960.4(FUS):c.1504_1505del (p.Asp502fs)|Deletion|Pathogenic|FUS|criteria provided, single submitter|16","280602|NM_004960.4(FUS):c.1510_1514dup (p.Phe506fs)|Duplication|Pathogenic|FUS|criteria provided, single submitter|16","2925592|NM_004960.4(FUS):c.1540A>G (p.Arg514Gly)|single nucleotide variant|Pathogenic|FUS|criteria provided, multiple submitters, no conflicts|16","2945054|NM_004960.4(FUS):c.1531dup (p.Met511fs)|Duplication|Pathogenic|FUS|criteria provided, single submitter|16","29707|NM_004960.4(FUS):c.1483C>T (p.Arg495Ter)|single nucleotide variant|Pathogenic|FUS|criteria provided, multiple submitters, no conflicts|16","29708|NM_004960.4(FUS):c.616G>A (p.Gly206Ser)|single nucleotide variant|Pathogenic|FUS|no assertion criteria provided|16","37070|NM_004960.4(FUS):c.868C>T (p.Gln290Ter)|single nucleotide variant|Pathogenic|FUS|no assertion criteria provided|16","3759352|NM_004960.4(FUS):c.1542G>T (p.Arg514Ser)|single nucleotide variant|Pathogenic|FUS|criteria provided, single submitter|16","3760171|NM_004960.4(FUS):c.1496del (p.Gly499fs)|Deletion|Pathogenic|FUS|criteria provided, single submitter|16","665141|NM_004960.4(FUS):c.1509_1510dup (p.Gly504fs)|Microsatellite|Pathogenic|FUS|criteria provided, single submitter|16","817574|NM_004960.4(FUS):c.1022_1023del (p.Ser340_Phe341insTer)|Deletion|Pathogenic|FUS|criteria provided, single submitter|16","847302|NM_004960.4(FUS):c.1541+1G>A|single nucleotide variant|Pathogenic|FUS|criteria provided, single submitter|16","873230|NM_004960.4(FUS):c.1394-1G>T|single nucleotide variant|Pathogenic|FUS|criteria provided, single submitter|16","873231|NM_004960.4(FUS):c.1555C>T (p.Gln519Ter)|single nucleotide variant|Pathogenic|FUS|criteria provided, single submitter|16","873234|NM_004960.4(FUS):c.1577A>G (p.Tyr526Cys)|single nucleotide variant|Pathogenic|FUS|criteria provided, single submitter|16","933229|NM_004960.4(FUS):c.1509dup (p.Gly504fs)|Duplication|Pathogenic|FUS|criteria provided, single submitter|16"]}]}