{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HGNC:3690,10,HGNC:3690,78,0]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:3690","source":"HGNC:3690|fibroblast growth factor receptor 3","targets":["1050565|NM_000142.5(FGFR3):c.940G>A (p.Ala314Thr)|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1065490|NM_000142.5(FGFR3):c.1954A>G (p.Thr652Ala)|single nucleotide variant|Pathogenic|FGFR3|criteria provided, single submitter|4","1163833|NM_000142.5(FGFR3):c.416A>C (p.Asp139Ala)|single nucleotide variant|Conflicting classifications of pathogenicity|FGFR3|criteria provided, conflicting classifications|4","1172560|NM_000142.5(FGFR3):c.1210A>G (p.Lys404Glu)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1174959|NM_000142.5(FGFR3):c.870C>T (p.His290=)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1176796|NM_000142.5(FGFR3):c.2066C>T (p.Thr689Met)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1182044|NM_000142.5(FGFR3):c.109+174T>C|single nucleotide variant|Benign|FGFR3|criteria provided, single submitter|4","1183225|NM_000142.5(FGFR3):c.1076-34dup|Duplication|Benign|FGFR3|criteria provided, single submitter|4","1187739|NM_000142.5(FGFR3):c.725C>T (p.Thr242Met)|single nucleotide variant|Conflicting classifications of pathogenicity|FGFR3|criteria provided, conflicting classifications|4","1187885|NM_000142.5(FGFR3):c.189G>A (p.Pro63=)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1187970|NM_000142.5(FGFR3):c.-102-181G>A|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1189295|NM_000142.5(FGFR3):c.2169-4G>A|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1189914|NM_000142.5(FGFR3):c.2360C>G (p.Ser787Cys)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1191305|NM_000142.5(FGFR3):c.1075+185G>A|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1192038|NM_000142.5(FGFR3):c.931-470C>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1192987|NM_000142.5(FGFR3):c.1266+64C>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1193084|NM_000142.5(FGFR3):c.2207C>A (p.Ser736Tyr)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1193773|NM_000142.5(FGFR3):c.1676C>T (p.Ala559Val)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1193915|NM_000142.5(FGFR3):c.885C>T (p.Gly295=)|single nucleotide variant|Conflicting classifications of pathogenicity|FGFR3|criteria provided, conflicting classifications|4","1195270|NM_000142.5(FGFR3):c.1900G>A (p.Ala634Thr)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1195496|NM_000142.5(FGFR3):c.110-218C>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1196039|NM_000142.5(FGFR3):c.2169-33G>A|single nucleotide variant|Benign/Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1196185|NM_000142.5(FGFR3):c.*140TG[3]|Microsatellite|Likely benign|FGFR3|criteria provided, single submitter|4","1197738|NM_000142.5(FGFR3):c.43G>T (p.Ala15Ser)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1199143|NM_000142.5(FGFR3):c.1076-41G>C|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1200590|NM_000142.5(FGFR3):c.*138C>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1200664|NM_000142.5(FGFR3):c.1206C>A (p.Pro402=)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1201990|NM_000142.5(FGFR3):c.2272G>A (p.Asp758Asn)|single nucleotide variant|Conflicting classifications of pathogenicity|FGFR3|criteria provided, conflicting classifications|4","1203329|NM_000142.5(FGFR3):c.1076-43G>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1204830|NM_000142.5(FGFR3):c.930+180G>A|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1204846|NM_000142.5(FGFR3):c.1674G>A (p.Ala558=)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1205724|NM_000142.5(FGFR3):c.534C>T (p.Ala178=)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1205823|NM_000142.5(FGFR3):c.380-101G>C|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1205996|NM_000142.5(FGFR3):c.1492C>T (p.Arg498Trp)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1206069|NM_000142.5(FGFR3):c.490C>G (p.Leu164Val)|single nucleotide variant|Benign/Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1206359|NM_000142.5(FGFR3):c.277C>T (p.Arg93Trp)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1208310|NM_000142.5(FGFR3):c.445+78C>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1212542|NM_000142.5(FGFR3):c.109+297C>A|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1212749|NM_000142.5(FGFR3):c.446-126C>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1213619|NM_000142.5(FGFR3):c.329G>A (p.Arg110Gln)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1215889|NM_000142.5(FGFR3):c.985G>A (p.Val329Ile)|single nucleotide variant|Conflicting classifications of pathogenicity|FGFR3|criteria provided, conflicting classifications|4","1216494|NM_000142.5(FGFR3):c.1076-42G>C|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1217558|NM_000142.5(FGFR3):c.*287C>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1218316|NM_000142.5(FGFR3):c.847C>A (p.Pro283Thr)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1218811|NM_000142.5(FGFR3):c.1182G>A (p.Thr394=)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1220220|NM_000142.5(FGFR3):c.1836+44C>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1223791|NM_000142.5(FGFR3):c.1075+168C>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1224374|NM_000142.5(FGFR3):c.370C>T (p.Arg124Trp)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1224453|NM_000142.5(FGFR3):c.937G>T (p.Gly313Cys)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1224471|NM_000142.5(FGFR3):c.685G>A (p.Val229Ile)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1224600|NM_000142.5(FGFR3):c.1960-13C>T|single nucleotide variant|Benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1227812|NM_000142.5(FGFR3):c.*36A>G|single nucleotide variant|Benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1229898|NM_000142.5(FGFR3):c.-102-18_-102-11del|Deletion|Benign/Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1251273|NM_000142.5(FGFR3):c.-103+141C>T|single nucleotide variant|Benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1252306|NM_000142.5(FGFR3):c.1285G>A (p.Ala429Thr)|single nucleotide variant|Benign/Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1253944|NM_000142.5(FGFR3):c.930+218G>A|single nucleotide variant|Benign|FGFR3|criteria provided, single submitter|4","1254285|NM_000142.5(FGFR3):c.1701G>C (p.Leu567=)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1254355|NM_000142.5(FGFR3):c.1195C>T (p.Arg399Cys)|single nucleotide variant|Conflicting classifications of pathogenicity|FGFR3|criteria provided, conflicting classifications|4","1254578|NM_000142.5(FGFR3):c.2249G>A (p.Arg750His)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1254762|NM_000142.5(FGFR3):c.921C>T (p.Thr307=)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1267087|NM_000142.5(FGFR3):c.930+174T>C|single nucleotide variant|Benign|FGFR3|criteria provided, single submitter|4","1270999|NM_000142.5(FGFR3):c.1076-34del|Deletion|Benign|FGFR3|criteria provided, single submitter|4","1280506|NM_000142.5(FGFR3):c.109+309C>T|single nucleotide variant|Benign|FGFR3|criteria provided, single submitter|4","1283657|NM_000142.5(FGFR3):c.1075+236T>C|single nucleotide variant|Benign|FGFR3|criteria provided, single submitter|4","1290748|NM_000142.5(FGFR3):c.*184C>T|single nucleotide variant|Benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1293252|NM_000142.5(FGFR3):c.*140TG[8]|Microsatellite|Benign|FGFR3|criteria provided, single submitter|4","1297603|NM_000142.5(FGFR3):c.1646-17G>A|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1297702|NM_000142.5(FGFR3):c.915C>T (p.Tyr305=)|single nucleotide variant|Likely benign|FGFR3|criteria provided, multiple submitters, no conflicts|4","1301520|NM_000142.5(FGFR3):c.932C>T (p.Thr311Met)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1303807|NM_000142.5(FGFR3):c.779C>T (p.Pro260Leu)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1303899|NM_000142.5(FGFR3):c.2349_2350del (p.Asp785fs)|Deletion|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1305219|NM_000142.5(FGFR3):c.43G>A (p.Ala15Thr)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1305323|NM_000142.5(FGFR3):c.1862G>T (p.Arg621Leu)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1305498|NM_000142.5(FGFR3):c.1675G>A (p.Ala559Thr)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1306088|NM_000142.5(FGFR3):c.1838G>A (p.Cys613Tyr)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1306204|NM_000142.5(FGFR3):c.2110_2126del (p.Phe704fs)|Deletion|Uncertain significance|FGFR3|criteria provided, single submitter|4","1306900|NM_000142.5(FGFR3):c.2374G>A (p.Asp792Asn)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1307191|NM_000142.5(FGFR3):c.585C>G (p.Phe195Leu)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1308572|NM_000142.5(FGFR3):c.781G>A (p.Ala261Thr)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1309204|NM_000142.5(FGFR3):c.2309del (p.Tyr770fs)|Deletion|Uncertain significance|FGFR3|criteria provided, single submitter|4","1309447|NM_000142.5(FGFR3):c.1242C>G (p.Ile414Met)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1309951|NM_000142.5(FGFR3):c.1255C>T (p.Leu419Phe)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1310286|NM_000142.5(FGFR3):c.1276G>A (p.Glu426Lys)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1310646|NM_000142.5(FGFR3):c.1547A>G (p.Asp516Gly)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1312813|NM_000142.5(FGFR3):c.630G>A (p.Gln210=)|single nucleotide variant|Conflicting classifications of pathogenicity|FGFR3|criteria provided, conflicting classifications|4","1313268|NM_000142.5(FGFR3):c.1921G>A (p.Asp641Asn)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1313374|NM_000142.5(FGFR3):c.707G>A (p.Ser236Asn)|single nucleotide variant|Conflicting classifications of pathogenicity|FGFR3|criteria provided, conflicting classifications|4","1314671|NM_000142.5(FGFR3):c.1646-11C>A|single nucleotide variant|Conflicting classifications of pathogenicity|FGFR3|criteria provided, conflicting classifications|4","1314866|NM_000142.5(FGFR3):c.2337del (p.Ser780fs)|Deletion|Uncertain significance|FGFR3|criteria provided, single submitter|4","1315094|NM_000142.5(FGFR3):c.965A>G (p.Glu322Gly)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1315100|NM_000142.5(FGFR3):c.202_204delinsT (p.Pro68fs)|Indel|Uncertain significance|FGFR3|criteria provided, single submitter|4","1315452|NM_000142.5(FGFR3):c.328C>T (p.Arg110Trp)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1319505|NM_000142.5(FGFR3):c.1959+6C>T|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1320855|NM_000142.5(FGFR3):c.446-10C>T|single nucleotide variant|Conflicting classifications of pathogenicity|FGFR3|criteria provided, conflicting classifications|4","1321739|NM_000142.5(FGFR3):c.1829C>A (p.Ser610Tyr)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, multiple submitters, no conflicts|4","1325830|NM_000142.5(FGFR3):c.1618A>C (p.Asn540His)|single nucleotide variant|Likely pathogenic|FGFR3|criteria provided, single submitter|4","1327391|NM_000142.5(FGFR3):c.1450G>A (p.Gly484Ser)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1328254|NM_000142.5(FGFR3):c.740-18C>T|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4","1328271|NM_000142.5(FGFR3):c.946A>G (p.Thr316Ala)|single nucleotide variant|Uncertain significance|FGFR3|criteria provided, single submitter|4","1328275|NM_000142.5(FGFR3):c.931-20G>A|single nucleotide variant|Likely benign|FGFR3|criteria provided, single submitter|4"]}]}