{"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:6893,10,HGNC:6893,6,1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:6893","source":"HGNC:6893|microtubule associated protein tau","targets":["1002664|NM_001377265.1(MAPT):c.1629C>G (p.Ile543Met)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1003702|NM_001377265.1(MAPT):c.1811C>A (p.Thr604Asn)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1037716|NM_001377265.1(MAPT):c.2286+6G>T|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1042712|NM_001377265.1(MAPT):c.1607G>A (p.Gly536Glu)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1061335|NM_001377265.1(MAPT):c.258A>C (p.Glu86Asp)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1099999|NM_001377265.1(MAPT):c.2418C>T (p.Thr806=)|single nucleotide variant|Likely benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1106245|NM_001377265.1(MAPT):c.2034C>T (p.Asn678=)|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1118038|NM_001377265.1(MAPT):c.1956C>T (p.Ile652=)|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1120381|NM_001377265.1(MAPT):c.2313C>A (p.Arg771=)|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1126880|NM_001377265.1(MAPT):c.1881G>A (p.Ser627=)|single nucleotide variant|Likely benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1158143|NM_001377265.1(MAPT):c.177G>C (p.Pro59=)|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1168309|NM_001377265.1(MAPT):c.-18+124C>G|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1169744|NM_001377265.1(MAPT):c.176C>T (p.Pro59Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|MAPT|criteria provided, conflicting classifications|17","1178457|NM_001377265.1(MAPT):c.1605+105T>C|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1182510|NM_001377265.1(MAPT):c.2173+34G>A|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1183434|NM_001377265.1(MAPT):c.221-94A>T|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1190317|NM_001377265.1(MAPT):c.220+2202G>A|single nucleotide variant|Likely benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1191111|NM_001377265.1(MAPT):c.-17-215C>T|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1193357|NM_001377265.1(MAPT):c.1733-31T>C|single nucleotide variant|Likely benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1198851|NM_001377265.1(MAPT):c.921C>G (p.Ser307=)|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1200135|NM_001377265.1(MAPT):c.427G>T (p.Ala143Ser)|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1200870|NM_001377265.1(MAPT):c.1732+195C>A|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1202465|NM_001377265.1(MAPT):c.1732+210dup|Duplication|Likely benign|MAPT|criteria provided, single submitter|17","1205763|NM_001377265.1(MAPT):c.1351+48_1351+56del|Microsatellite|Likely benign|MAPT|criteria provided, single submitter|17","1209396|NM_001377265.1(MAPT):c.1351+21C>T|single nucleotide variant|Likely benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1209432|NM_001377265.1(MAPT):c.464G>A (p.Arg155His)|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1209906|NM_001377265.1(MAPT):c.1326C>T (p.Pro442=)|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1209982|NM_001377265.1(MAPT):c.220+2477C>G|single nucleotide variant|Likely benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1210047|NM_001377265.1(MAPT):c.220+2432G>A|single nucleotide variant|Benign/Likely benign|MAPT|no assertion criteria provided|17","1210744|NM_001377265.1(MAPT):c.1352-103C>T|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1211081|NM_001377265.1(MAPT):c.1351+52C>T|single nucleotide variant|Likely benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1213569|NM_001377265.1(MAPT):c.2286+109G>C|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1217746|NM_001377265.1(MAPT):c.1998+147C>T|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1218907|NM_001377265.1(MAPT):c.2092-192C>T|single nucleotide variant|Likely benign|MAPT|criteria provided, single submitter|17","1221560|NM_001377265.1(MAPT):c.1999-47C>A|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1222027|NM_001377265.1(MAPT):c.220+2613G>A|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1222642|NM_001377265.1(MAPT):c.1605+67A>G|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1224063|NM_001377265.1(MAPT):c.220+239G>A|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1225942|NM_001377265.1(MAPT):c.2173+196C>T|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1227529|NM_001377265.1(MAPT):c.1352-72T>C|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1227841|NM_001377265.1(MAPT):c.1408-249C>T|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1229021|NM_001377265.1(MAPT):c.1606-283G>A|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1229604|NM_001377265.1(MAPT):c.1408-198G>A|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1229674|NM_001377265.1(MAPT):c.1998+103G>A|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1230922|NM_001377265.1(MAPT):c.134-284_134-281del|Deletion|Benign|MAPT|criteria provided, single submitter|17","1232415|NM_001377265.1(MAPT):c.1605+241G>A|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1236004|NM_001377265.1(MAPT):c.1606-334A>G|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1238355|NM_001377265.1(MAPT):c.1407+298_1407+299insGGACAGTAAATGAAGGTGTGTTTGAAAACCAAC|Insertion|Benign|MAPT|criteria provided, single submitter|17","1239288|NM_001377265.1(MAPT):c.1352-198G>A|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1242653|NM_001377265.1(MAPT):c.-17-171G>T|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1250153|NM_001377265.1(MAPT):c.134-92T>C|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1253635|NM_001377265.1(MAPT):c.1732+246C>T|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1256161|NM_001377265.1(MAPT):c.2090G>T (p.Ser697Ile)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1256742|NM_001377265.1(MAPT):c.303G>A (p.Pro101=)|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1259075|NM_001377265.1(MAPT):c.-17-322C>T|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1261272|NM_001377265.1(MAPT):c.286+291C>G|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1263140|NM_001377265.1(MAPT):c.134-287del|Deletion|Benign|MAPT|criteria provided, single submitter|17","1263930|NM_001377265.1(MAPT):c.2174-257dup|Duplication|Benign|MAPT|criteria provided, single submitter|17","1266638|NM_001377265.1(MAPT):c.134-290_134-289insACCA|Insertion|Benign|MAPT|criteria provided, single submitter|17","1266777|NM_001377265.1(MAPT):c.1733-26G>A|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1267393|NM_001377265.1(MAPT):c.2174-323T>G|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1267707|NM_001377265.1(MAPT):c.133+284C>T|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1268666|NM_001377265.1(MAPT):c.1732+228C>G|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1270290|NM_001377265.1(MAPT):c.220+2301A>G|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1270750|NM_001377265.1(MAPT):c.221-103T>A|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1271108|NM_001377265.1(MAPT):c.2074G>A (p.Val692Ile)|single nucleotide variant|Benign/Likely benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1272983|NM_001377265.1(MAPT):c.220+2698T>C|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1276777|NM_001377265.1(MAPT):c.1407+297_1407+298insCCCC|Insertion|Benign|MAPT|criteria provided, single submitter|17","1282324|NM_001377265.1(MAPT):c.220+2278T>G|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1287204|NM_001377265.1(MAPT):c.1351+315del|Deletion|Benign|MAPT|criteria provided, single submitter|17","1293130|NM_001377265.1(MAPT):c.220+2277C>G|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1295196|NM_001377265.1(MAPT):c.1999-176A>G|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1295197|NM_001377265.1(MAPT):c.1351+249A>C|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1295198|NM_001377265.1(MAPT):c.2173+90G>A|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1295200|NM_001377265.1(MAPT):c.1999-168G>A|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1295309|NM_001377265.1(MAPT):c.547G>A (p.Glu183Lys)|single nucleotide variant|Benign|MAPT|criteria provided, multiple submitters, no conflicts|17","1295681|NM_001377265.1(MAPT):c.1732+2137C>G|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1296619|NM_001377265.1(MAPT):c.-17-277A>G|single nucleotide variant|Benign|MAPT|criteria provided, single submitter|17","1298709|NM_001377265.1(MAPT):c.1011G>C (p.Glu337Asp)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1298710|NM_001377265.1(MAPT):c.1762G>A (p.Gly588Ser)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, multiple submitters, no conflicts|17","1302562|NM_001377265.1(MAPT):c.110G>T (p.Gly37Val)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1308215|NM_001377265.1(MAPT):c.898G>A (p.Asp300Asn)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1333780|NM_001377265.1(MAPT):c.1814C>T (p.Pro605Leu)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1335279|NM_001377265.1(MAPT):c.25G>A (p.Glu9Lys)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, multiple submitters, no conflicts|17","1345546|NM_001377265.1(MAPT):c.10C>A (p.Pro4Thr)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, multiple submitters, no conflicts|17","1354263|NM_001377265.1(MAPT):c.2344G>A (p.Ala782Thr)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1365252|NM_001377265.1(MAPT):c.232G>A (p.Gly78Ser)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1368749|NM_001377265.1(MAPT):c.60G>C (p.Leu20Phe)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1372289|NM_001377265.1(MAPT):c.2428G>A (p.Asp810Asn)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1413319|NM_001377265.1(MAPT):c.1808G>A (p.Arg603His)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1414056|NM_001377265.1(MAPT):c.1364G>A (p.Ser455Asn)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1416826|NM_001377265.1(MAPT):c.1355G>A (p.Arg452His)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, single submitter|17","1417517|NM_001377265.1(MAPT):c.1807C>T (p.Arg603Cys)|single nucleotide variant|Uncertain significance|MAPT|criteria provided, multiple submitters, no conflicts|17","1424259|NM_001377265.1(MAPT):c.80G>A (p.Gly27Glu)|single nucleotide variant|Conflicting classifications of pathogenicity|MAPT|criteria provided, conflicting classifications|17","14245|NM_001377265.1(MAPT):c.2078C>T (p.Pro693Leu)|single nucleotide variant|Pathogenic|MAPT|criteria provided, multiple submitters, no conflicts|17","14246|NM_001377265.1(MAPT):c.1991G>T (p.Gly664Val)|single nucleotide variant|Pathogenic|MAPT|no assertion criteria provided|17","14247|NM_001377265.1(MAPT):c.2392C>T (p.Arg798Trp)|single nucleotide variant|Pathogenic|MAPT|criteria provided, multiple submitters, no conflicts|17","14248|NM_001377265.1(MAPT):c.2091+14C>T|single nucleotide variant|Pathogenic|MAPT|no assertion criteria provided|17","14251|NM_001377265.1(MAPT):c.2091+1G>A|single nucleotide variant|Pathogenic|MAPT|no assertion criteria provided|17","14252|NM_001377265.1(MAPT):c.2185G>A (p.Val729Met)|single nucleotide variant|Pathogenic|MAPT|criteria provided, multiple submitters, no conflicts|17"]}]}