{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":14,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:3690","source":"HGNC:3690|fibroblast growth factor receptor 3","targets":["1325830|NM_000142.5(FGFR3):c.1618A>C (p.Asn540His)|single nucleotide variant|Likely pathogenic|FGFR3|criteria provided, single submitter|4","1332776|NM_000142.5(FGFR3):c.1144G>A (p.Gly382Ser)|single nucleotide variant|Likely pathogenic|FGFR3|criteria provided, single submitter|4","155481|GRCh38/hg38 4p16.3(chr4:1699291-1973304)x1|copy number loss|Likely pathogenic|FGFR3|no assertion criteria provided|4","1679899|NM_000142.5(FGFR3):c.1183C>A (p.Leu395Ile)|single nucleotide variant|Likely pathogenic|FGFR3|criteria provided, single submitter|4","1680048|NM_000142.5(FGFR3):c.970C>G (p.Leu324Val)|single nucleotide variant|Likely pathogenic|FGFR3|criteria provided, single submitter|4","2429355|NM_000142.5(FGFR3):c.1633_1634del (p.Cys545fs)|Deletion|Likely pathogenic|FGFR3|no assertion criteria provided|4","2502296|NM_000142.5(FGFR3):c.977T>G (p.Leu326Trp)|single nucleotide variant|Likely pathogenic|FGFR3|criteria provided, single submitter|4","3342383|NM_000142.5(FGFR3):c.2408del (p.Gly803fs)|Deletion|Likely pathogenic|FGFR3|criteria provided, single submitter|4","4056874|NM_000142.5(FGFR3):c.746C>A (p.Ser249Tyr)|single nucleotide variant|Likely pathogenic|FGFR3|criteria provided, single submitter|4","423158|NM_000142.5(FGFR3):c.2407_*5delinsCCCTG (p.Gly803_Ter807delinsProXaa)|Indel|Likely pathogenic|FGFR3|criteria provided, single submitter|4","495323|NC_000004.12:g.1735761_1806926dup|Duplication|Likely pathogenic|FGFR3|no assertion criteria provided|4","562877|GRCh37/hg19 4p16.3(chr4:1770486-2303110)x3|copy number gain|Likely pathogenic|FGFR3|no assertion criteria provided|4","627445|NM_000142.5(FGFR3):c.2287C>T (p.Leu763=)|single nucleotide variant|Likely pathogenic|FGFR3|no assertion criteria provided|4","65561|NM_000142.5(FGFR3):c.2419T>C (p.Ter807Arg)|single nucleotide variant|Likely pathogenic|FGFR3|criteria provided, single submitter|4"]}]}