{"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:644,10,HGNC:644,141,-1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:644","source":"HGNC:644|androgen receptor","targets":["1020251|NM_000044.6(AR):c.2318A>T (p.Glu773Val)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1025856|NM_000044.6(AR):c.2334G>T (p.Lys778Asn)|single nucleotide variant|Uncertain significance|AR|criteria provided, multiple submitters, no conflicts|X","1030549|NM_000044.6(AR):c.631G>A (p.Ala211Thr)|single nucleotide variant|Uncertain significance|AR|criteria provided, multiple submitters, no conflicts|X","1030550|NM_000044.6(AR):c.847C>T (p.Pro283Ser)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1035174|NM_000044.6(AR):c.2383T>G (p.Phe795Val)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1044220|NM_000044.6(AR):c.1994T>C (p.Ile665Thr)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1049223|NM_000044.6(AR):c.170T>A (p.Leu57Gln)|single nucleotide variant|Benign/Likely benign|AR|criteria provided, multiple submitters, no conflicts|X","1053541|NM_000044.6(AR):c.2741C>A (p.Pro914His)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1062965|NM_000044.6(AR):c.2159C>T (p.Ala720Val)|single nucleotide variant|Conflicting classifications of pathogenicity|AR|criteria provided, conflicting classifications|X","1063718|NM_000044.6(AR):c.1889G>A (p.Arg630Gln)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1065434|NM_000044.6(AR):c.2237T>C (p.Met746Thr)|single nucleotide variant|Pathogenic/Likely pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1068775|NM_000044.6(AR):c.2225G>T (p.Trp742Leu)|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1071361|NC_000023.10:g.(?_66905832)_(66905988_?)del|Deletion|Pathogenic|AR|criteria provided, single submitter|X","1071362|NC_000023.10:g.(?_66863078)_(66943703_?)del|Deletion|Pathogenic|AR|criteria provided, single submitter|X","1072748|NM_000044.6(AR):c.1737del (p.Cys580fs)|Deletion|Pathogenic|AR|criteria provided, single submitter|X","1076800|NM_000044.6(AR):c.1063G>T (p.Glu355Ter)|single nucleotide variant|Pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1077100|NM_000044.6(AR):c.2170C>T (p.Pro724Ser)|single nucleotide variant|Pathogenic/Likely pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1111146|NM_000044.6(AR):c.1125G>C (p.Pro375=)|single nucleotide variant|Likely benign|AR|criteria provided, single submitter|X","1166167|NM_000044.6(AR):c.171GCA[13] (p.Gln71_Gln80del)|Microsatellite|Benign/Likely benign|AR|criteria provided, multiple submitters, no conflicts|X","1166192|NM_000044.6(AR):c.2388A>G (p.Gly796=)|single nucleotide variant|Benign|AR|criteria provided, single submitter|X","1166508|NM_000044.6(AR):c.1370GCG[10] (p.Gly467_Gly473del)|Microsatellite|Benign|AR|criteria provided, multiple submitters, no conflicts|X","1167626|NM_000044.6(AR):c.1301C>T (p.Ser434Phe)|single nucleotide variant|Conflicting classifications of pathogenicity|AR|criteria provided, conflicting classifications|X","1167648|NM_000044.6(AR):c.1370GCG[9] (p.Gly466_Gly473del)|Microsatellite|Benign|AR|criteria provided, single submitter|X","1168151|NM_000044.6(AR):c.171GCA[27] (p.Gln77_Gln80dup)|Microsatellite|Benign/Likely benign|AR|criteria provided, multiple submitters, no conflicts|X","1168650|NM_000044.6(AR):c.324G>C (p.Leu108=)|single nucleotide variant|Benign/Likely benign|AR|criteria provided, multiple submitters, no conflicts|X","1168910|NM_000044.6(AR):c.1370GCG[11] (p.Gly468_Gly473del)|Microsatellite|Benign|AR|criteria provided, multiple submitters, no conflicts|X","1169430|NM_000044.6(AR):c.1370_1371insTGGCGGCGG (p.Gly471_Gly473dup)|Insertion|Benign|AR|criteria provided, single submitter|X","1169431|NM_000044.6(AR):c.1370_1371insTGGCGGCGGCGG (p.Gly470_Gly473dup)|Insertion|Benign|AR|criteria provided, multiple submitters, no conflicts|X","1170227|NM_000044.6(AR):c.1788C>T (p.Cys596=)|single nucleotide variant|Benign|AR|criteria provided, multiple submitters, no conflicts|X","1177442|NM_000044.6(AR):c.2255G>C (p.Trp752Ser)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1183563|NM_000044.6(AR):c.2318+243A>G|single nucleotide variant|Benign|AR|criteria provided, single submitter|X","1189467|NM_000044.6(AR):c.171GCA[35] (p.Gln69_Gln80dup)|Microsatellite|Likely benign|AR|criteria provided, multiple submitters, no conflicts|X","1196069|NM_000044.6(AR):c.1885+4A>T|single nucleotide variant|Conflicting classifications of pathogenicity|AR|criteria provided, conflicting classifications|X","1196591|NM_000044.6(AR):c.1762G>C (p.Ala588Pro)|single nucleotide variant|Pathogenic/Likely pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1200448|NM_000044.6(AR):c.171GCA[34] (p.Gln70_Gln80dup)|Microsatellite|Likely benign|AR|criteria provided, single submitter|X","1202466|NM_000044.6(AR):c.1616+22453G>T|single nucleotide variant|Likely benign|AR|criteria provided, multiple submitters, no conflicts|X","1202584|NM_000044.6(AR):c.2607+2T>G|single nucleotide variant|Pathogenic|AR|no assertion criteria provided|X","1202585|NM_000044.6(AR):c.2657A>T (p.His886Leu)|single nucleotide variant|Pathogenic|AR|no assertion criteria provided|X","1204465|NM_000044.6(AR):c.2608-165AC[13]|Microsatellite|Likely benign|AR|criteria provided, single submitter|X","1205841|NM_000044.6(AR):c.814C>T (p.Leu272Phe)|single nucleotide variant|Conflicting classifications of pathogenicity|AR|criteria provided, conflicting classifications|X","1207735|NM_000044.6(AR):c.2450-42G>A|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1213203|NM_000044.6(AR):c.1186G>A (p.Gly396Ser)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1232036|NM_000044.6(AR):c.1371C>T (p.Gly457=)|single nucleotide variant|Benign/Likely benign|AR|criteria provided, multiple submitters, no conflicts|X","1237904|NM_000044.6(AR):c.1886-207A>T|single nucleotide variant|Benign|AR|criteria provided, multiple submitters, no conflicts|X","1239857|NM_000044.6(AR):c.2319-78T>G|single nucleotide variant|Benign|AR|criteria provided, multiple submitters, no conflicts|X","1244234|NM_000044.6(AR):c.1792A>G (p.Ser598Gly)|single nucleotide variant|Conflicting classifications of pathogenicity|AR|criteria provided, conflicting classifications|X","1244244|NM_000044.6(AR):c.2486A>T (p.Asp829Val)|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1245219|NM_000044.6(AR):c.2608-165AC[15]|Microsatellite|Benign|AR|criteria provided, single submitter|X","1257319|NM_000044.6(AR):c.231_232insGCAGCAGCA (p.Gln77_Gln78insAlaAlaAla)|Insertion|Benign|AR|criteria provided, single submitter|X","1259529|NM_000044.6(AR):c.2450-44G>A|single nucleotide variant|Benign|AR|criteria provided, multiple submitters, no conflicts|X","1273615|NM_000044.6(AR):c.1768+204T>G|single nucleotide variant|Benign|AR|criteria provided, single submitter|X","1276396|NM_000044.6(AR):c.2608-165AC[14]|Microsatellite|Benign|AR|criteria provided, single submitter|X","1276845|NM_000044.6(AR):c.171GCA[21] (p.Gln79_Gln80del)|Microsatellite|Benign|AR|criteria provided, multiple submitters, no conflicts|X","1279480|NM_000044.6(AR):c.1617-255A>G|single nucleotide variant|Benign|AR|criteria provided, single submitter|X","1285161|NM_000044.6(AR):c.171GCA[29] (p.Gln75_Gln80dup)|Microsatellite|Benign/Likely benign|AR|criteria provided, multiple submitters, no conflicts|X","1288845|NM_000044.6(AR):c.2318+285A>G|single nucleotide variant|Benign|AR|criteria provided, single submitter|X","1298359|NM_000044.6(AR):c.2255G>A (p.Trp752Ter)|single nucleotide variant|Pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1298364|NM_000044.6(AR):c.1567G>T (p.Glu523Ter)|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1298366|NM_000044.6(AR):c.1742A>C (p.Lys581Thr)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1298367|NM_000044.6(AR):c.175C>T (p.Gln59Ter)|single nucleotide variant|Pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1299195|NM_000044.6(AR):c.1370GCG[4] (p.Gly461_Gly473del)|Microsatellite|Benign|AR|criteria provided, single submitter|X","1299381|NM_000044.6(AR):c.1927G>A (p.Glu643Lys)|single nucleotide variant|Uncertain significance|AR|no assertion criteria provided|X","1323926|NM_000044.6(AR):c.649del (p.Ala217fs)|Deletion|Likely pathogenic|AR|criteria provided, single submitter|X","1333387|NM_000044.6(AR):c.2710G>T (p.Val904Leu)|single nucleotide variant|Pathogenic/Likely pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1333500|NM_000044.6(AR):c.2078A>T (p.Asn693Ile)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1336058|NM_000044.6(AR):c.1029T>C (p.Ser343=)|single nucleotide variant|Benign|AR|criteria provided, multiple submitters, no conflicts|X","1337825|NM_000044.6(AR):c.1380C>T (p.Gly460=)|single nucleotide variant|Likely benign|AR|criteria provided, multiple submitters, no conflicts|X","1338469|NM_000044.6(AR):c.2197G>A (p.Asp733Asn)|single nucleotide variant|Pathogenic/Likely pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1338498|NM_000044.6(AR):c.675_678del (p.Asn224_Tyr225insTer)|Deletion|Pathogenic|AR|criteria provided, single submitter|X","1338547|NM_000044.6(AR):c.170delinsAGCA (p.Leu57delinsGlnGln)|Indel|Likely benign|AR|criteria provided, single submitter|X","1338633|NM_000044.6(AR):c.2668G>T (p.Val890Leu)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X","1338786|NM_000044.6(AR):c.1616+22263G>A|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1339111|NM_000044.6(AR):c.2227A>G (p.Met743Val)|single nucleotide variant|Conflicting classifications of pathogenicity|AR|criteria provided, conflicting classifications|X","1339160|NM_000044.6(AR):c.2726C>T (p.Ser909Phe)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1340798|GRCh37/hg19 Xq12-13.1(chrX:66803179-67815570)x2|copy number gain|Uncertain significance|AR|no assertion criteria provided|X","1341194|GRCh37/hg19 Xq12(chrX:66911061-67264952)x2|copy number gain|Uncertain significance|AR|no assertion criteria provided|X","1341693|NM_000044.6(AR):c.2226G>A (p.Trp742Ter)|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1342730|NM_000044.6(AR):c.2494C>T (p.Arg832Ter)|single nucleotide variant|Pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1344487|NM_000044.6(AR):c.2126G>A (p.Gly709Glu)|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1344505|NM_000044.6(AR):c.2407dup (p.Gln803fs)|Duplication|Pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1366022|NM_000044.6(AR):c.1768+3A>G|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1368614|NM_000044.6(AR):c.1443C>A (p.Tyr481Ter)|single nucleotide variant|Pathogenic/Likely pathogenic|AR|criteria provided, multiple submitters, no conflicts|X","1389477|NM_000044.6(AR):c.2360G>C (p.Arg787Pro)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1394063|NM_000044.6(AR):c.2319_2321dup (p.Tyr774Ter)|Duplication|Pathogenic|AR|criteria provided, single submitter|X","1403739|NM_000044.6(AR):c.172_173insTGCAGCAGCAGCAGCAGCAGC (p.Leu57_Gln58insLeuGlnGlnGlnGlnGlnGln)|Insertion|Uncertain significance|AR|criteria provided, single submitter|X","1410073|NM_000044.6(AR):c.2653T>C (p.Ser885Pro)|single nucleotide variant|Uncertain significance|AR|criteria provided, single submitter|X","1410848|NM_000044.6(AR):c.1477C>T (p.Gln493Ter)|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1421027|NM_000044.6(AR):c.358C>T (p.Gln120Ter)|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1421729|NM_000044.6(AR):c.1370GCG[6] (p.Gly463_Gly473del)|Microsatellite|Uncertain significance|AR|criteria provided, single submitter|X","1428356|NM_000044.6(AR):c.170AGC[8] (p.Leu56_Leu57insGlnGlnGlnGlnGlnGlnGlnGln)|Microsatellite|Uncertain significance|AR|criteria provided, single submitter|X","1437090|NM_000044.6(AR):c.1885+2T>G|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1454388|NC_000023.10:g.(?_66941655)_(66943683_?)del|Deletion|Pathogenic|AR|criteria provided, single submitter|X","1454419|NM_000044.6(AR):c.1707del (p.Cys570fs)|Deletion|Pathogenic|AR|criteria provided, single submitter|X","1454671|NM_000044.6(AR):c.829_833dup (p.Val279fs)|Duplication|Pathogenic|AR|criteria provided, single submitter|X","1455502|NM_000044.6(AR):c.2512G>T (p.Glu838Ter)|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1460010|NC_000023.10:g.(?_66931224)_(66931551_?)del|Deletion|Pathogenic|AR|criteria provided, single submitter|X","1460367|NM_000044.6(AR):c.2515C>A (p.Leu839Ile)|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1468498|NM_000044.6(AR):c.1419_1421del (p.Glu474del)|Deletion|Uncertain significance|AR|criteria provided, single submitter|X","1470535|NM_000044.6(AR):c.1A>T (p.Met1Leu)|single nucleotide variant|Pathogenic|AR|criteria provided, single submitter|X","1480317|NM_000044.6(AR):c.2318A>G (p.Glu773Gly)|single nucleotide variant|Likely pathogenic|AR|criteria provided, single submitter|X"]}]}