{"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:4010,10,HGNC:4010,105,1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:4010","source":"HGNC:4010|FUS RNA binding protein","targets":["1001437|NM_004960.4(FUS):c.1552A>G (p.Arg518Gly)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1013097|NM_004960.4(FUS):c.181A>G (p.Ser61Gly)|single nucleotide variant|Uncertain significance|FUS|criteria provided, multiple submitters, no conflicts|16","1013098|NM_004960.4(FUS):c.608G>A (p.Gly203Asp)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1040027|NM_004960.4(FUS):c.493A>G (p.Ser165Gly)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1045687|NM_004960.4(FUS):c.265T>A (p.Ser89Thr)|single nucleotide variant|Uncertain significance|FUS|criteria provided, multiple submitters, no conflicts|16","1054806|NM_004960.4(FUS):c.1317T>C (p.Ser439=)|single nucleotide variant|Conflicting classifications of pathogenicity|FUS|criteria provided, conflicting classifications|16","1073222|NM_004960.4(FUS):c.1554_1557del (p.Gln519fs)|Microsatellite|Pathogenic|FUS|criteria provided, multiple submitters, no conflicts|16","1077589|NM_004960.4(FUS):c.684_692del (p.Gly229_Gly231del)|Deletion|Conflicting classifications of pathogenicity|FUS|criteria provided, conflicting classifications|16","1091213|NM_004960.4(FUS):c.231G>A (p.Ser77=)|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1113414|NM_004960.4(FUS):c.52C>A (p.Pro18Thr)|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1137954|NM_004960.4(FUS):c.1452C>T (p.Tyr484=)|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1148671|NM_004960.4(FUS):c.1169-7G>A|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1160728|NM_004960.4(FUS):c.375C>G (p.Pro125=)|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1167570|NM_004960.4(FUS):c.66G>A (p.Gly22=)|single nucleotide variant|Benign/Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1182870|NM_004960.4(FUS):c.1542-5del|Deletion|Likely benign|FUS|criteria provided, single submitter|16","1187752|NM_004960.4(FUS):c.190+261A>C|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1189075|NM_004960.4(FUS):c.190+173C>G|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1189317|NM_004960.4(FUS):c.1393+34G>T|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1194586|NM_004960.4(FUS):c.191-23C>G|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1195860|NM_004960.4(FUS):c.523+172C>T|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1198528|NM_004960.4(FUS):c.190+241G>A|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1199202|NM_004960.4(FUS):c.824A>G (p.His275Arg)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1199757|NM_004960.4(FUS):c.523+248C>G|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1200398|NM_004960.4(FUS):c.1542-5dup|Duplication|Likely benign|FUS|criteria provided, single submitter|16","1201317|NC_000016.10:g.31180051C>T|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1201558|NM_004960.4(FUS):c.833-284A>T|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1201681|NM_004960.4(FUS):c.190+216C>T|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1203951|NM_004960.4(FUS):c.190+251C>T|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1204289|NM_004960.4(FUS):c.1542-97G>T|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1204463|NM_004960.4(FUS):c.833-43A>G|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1208458|NM_004960.4(FUS):c.833-242G>T|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1209969|NM_004960.4(FUS):c.1542-6_1542-5del|Deletion|Benign/Likely benign|FUS|no assertion criteria provided|16","1212742|NM_004960.4(FUS):c.800-275C>G|single nucleotide variant|Benign/Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1213403|NM_004960.4(FUS):c.167CTT[1] (p.Ser57del)|Microsatellite|Conflicting classifications of pathogenicity|FUS|criteria provided, conflicting classifications|16","1218785|NM_004960.4(FUS):c.833-29C>T|single nucleotide variant|Benign/Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1231946|NM_004960.4(FUS):c.799+179G>C|single nucleotide variant|Benign|FUS|criteria provided, multiple submitters, no conflicts|16","1236086|NM_004960.4(FUS):c.1541+125A>T|single nucleotide variant|Benign|FUS|criteria provided, multiple submitters, no conflicts|16","1239588|NM_004960.4(FUS):c.190+197T>C|single nucleotide variant|Benign|FUS|criteria provided, multiple submitters, no conflicts|16","1247590|NM_004960.4(FUS):c.523+59del|Deletion|Benign|FUS|criteria provided, single submitter|16","1247717|NM_004960.4(FUS):c.832+221G>T|single nucleotide variant|Benign|FUS|criteria provided, multiple submitters, no conflicts|16","1251703|NM_004960.4(FUS):c.524-112_524-102del|Deletion|Benign|FUS|criteria provided, single submitter|16","1256129|NM_004960.3(FUS):c.515_523+3del|Microsatellite|Conflicting classifications of pathogenicity|FUS|criteria provided, conflicting classifications|16","1258403|NM_004960.4(FUS):c.523+48T>C|single nucleotide variant|Benign|FUS|criteria provided, single submitter|16","1270494|NM_004960.4(FUS):c.523+42C>T|single nucleotide variant|Benign|FUS|criteria provided, single submitter|16","1274030|NM_004960.4(FUS):c.765-25C>T|single nucleotide variant|Benign|FUS|criteria provided, single submitter|16","1281612|NM_004960.4(FUS):c.1067-52G>A|single nucleotide variant|Benign|FUS|criteria provided, multiple submitters, no conflicts|16","1286509|NM_004960.4(FUS):c.800-26dup|Duplication|Benign|FUS|criteria provided, single submitter|16","1293274|NM_004960.4(FUS):c.800-247G>T|single nucleotide variant|Benign|FUS|criteria provided, multiple submitters, no conflicts|16","1293275|NM_004960.4(FUS):c.524-155T>C|single nucleotide variant|Benign|FUS|criteria provided, single submitter|16","1295730|NM_004960.4(FUS):c.523+59dup|Duplication|Benign|FUS|criteria provided, single submitter|16","1295926|NM_004960.4(FUS):c.523+22C>T|single nucleotide variant|Benign/Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1298663|NM_004960.4(FUS):c.*65_*66del|Deletion|Uncertain significance|FUS|criteria provided, single submitter|16","1315606|NM_004960.4(FUS):c.*59G>A|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1318646|NM_004960.4(FUS):c.523+112A>G|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1318851|NM_004960.4(FUS):c.595C>G (p.Gln199Glu)|single nucleotide variant|Uncertain significance|FUS|criteria provided, multiple submitters, no conflicts|16","1320885|NM_004960.4(FUS):c.940A>G (p.Asn314Asp)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1328656|NM_004960.4(FUS):c.832+46C>G|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1333381|NM_004960.4(FUS):c.1542-1G>C|single nucleotide variant|Likely pathogenic|FUS|criteria provided, single submitter|16","1335212|NM_004960.4(FUS):c.-44G>A|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1339102|NM_004960.4(FUS):c.1573C>G (p.Pro525Ala)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1350525|NM_004960.4(FUS):c.669CGG[10] (p.Gly228_Gly231dup)|Microsatellite|Uncertain significance|FUS|criteria provided, single submitter|16","1357166|NM_004960.4(FUS):c.215C>T (p.Pro72Leu)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1377485|NM_004960.4(FUS):c.691G>A (p.Gly231Ser)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1386031|NM_004960.4(FUS):c.652_678del (p.Arg218_Gly226del)|Deletion|Uncertain significance|FUS|criteria provided, single submitter|16","1390161|NM_004960.4(FUS):c.649G>C (p.Gly217Arg)|single nucleotide variant|Uncertain significance|FUS|criteria provided, multiple submitters, no conflicts|16","1415706|NM_004960.4(FUS):c.669CGG[9] (p.Gly229_Gly231dup)|Microsatellite|Conflicting classifications of pathogenicity|FUS|criteria provided, conflicting classifications|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","1470908|NM_004960.4(FUS):c.1471C>A (p.Arg491Ser)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1485282|NM_004960.4(FUS):c.1391_1392dup (p.Gly465fs)|Duplication|Pathogenic|FUS|criteria provided, single submitter|16","1509772|NM_004960.4(FUS):c.1147C>T (p.Arg383Cys)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1518792|NM_004960.4(FUS):c.716A>G (p.Tyr239Cys)|single nucleotide variant|Uncertain significance|FUS|criteria provided, multiple submitters, no conflicts|16","1519291|NM_004960.4(FUS):c.484A>C (p.Asn162His)|single nucleotide variant|Conflicting classifications of pathogenicity|FUS|criteria provided, conflicting classifications|16","1530335|NM_004960.4(FUS):c.47C>T (p.Ala16Val)|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1539279|NM_004960.4(FUS):c.300T>C (p.Tyr100=)|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1549061|NM_004960.4(FUS):c.96C>T (p.Pro32=)|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1562215|NM_004960.4(FUS):c.726A>G (p.Arg242=)|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1567449|NM_004960.4(FUS):c.99C>T (p.Tyr33=)|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1581652|NM_004960.4(FUS):c.318C>T (p.Pro106=)|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1594850|NM_004960.4(FUS):c.335+19C>T|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1599236|NM_004960.4(FUS):c.524-13dup|Duplication|Benign/Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1599440|NM_004960.4(FUS):c.336-19_336-18insG|Insertion|Benign/Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1601917|NM_004960.4(FUS):c.39-11C>G|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1620071|NM_004960.4(FUS):c.936+21dup|Duplication|Likely benign|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","16226|NM_004960.4(FUS):c.1520G>A (p.Gly507Asp)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","16227|NM_004960.4(FUS):c.646C>T (p.Arg216Cys)|single nucleotide variant|Conflicting classifications of pathogenicity|FUS|criteria provided, conflicting classifications|16","16228|NM_004960.4(FUS):c.1570A>T (p.Arg524Trp)|single nucleotide variant|Uncertain significance|FUS|criteria provided, single submitter|16","1628437|NM_004960.4(FUS):c.799+13A>T|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1630018|NM_004960.4(FUS):c.648C>T (p.Arg216=)|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1631768|NM_004960.4(FUS):c.543A>G (p.Gln181=)|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1632061|NM_004960.4(FUS):c.833-17C>T|single nucleotide variant|Benign|FUS|criteria provided, single submitter|16","1656122|NM_004960.4(FUS):c.336-19_336-16del|Deletion|Benign|FUS|criteria provided, single submitter|16","1659951|NM_004960.4(FUS):c.1014G>T (p.Thr338=)|single nucleotide variant|Likely benign|FUS|criteria provided, single submitter|16","1669202|NM_004960.4(FUS):c.1461C>T (p.Arg487=)|single nucleotide variant|Likely benign|FUS|criteria provided, multiple submitters, no conflicts|16","1676221|NM_004960.4(FUS):c.1493G>A (p.Arg498Gln)|single nucleotide variant|Uncertain significance|FUS|criteria provided, multiple submitters, no conflicts|16"]}]}