{"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:11110,10,HGNC:11110,198,0]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:11110","source":"HGNC:11110|AT-rich interaction domain 1A","targets":["1012517|NM_006015.6(ARID1A):c.357G>A (p.Glu119=)|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1012518|NM_006015.6(ARID1A):c.5125C>T (p.Leu1709Phe)|single nucleotide variant|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1028989|NM_006015.6(ARID1A):c.1712C>T (p.Ser571Leu)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, multiple submitters, no conflicts|1","1028990|NM_006015.6(ARID1A):c.2756A>G (p.Asn919Ser)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1028991|NM_006015.6(ARID1A):c.289G>A (p.Glu97Lys)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1028992|NM_006015.6(ARID1A):c.3049G>A (p.Glu1017Lys)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, multiple submitters, no conflicts|1","1028993|NM_006015.6(ARID1A):c.326C>G (p.Pro109Arg)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1028994|NM_006015.6(ARID1A):c.3276G>T (p.Leu1092Phe)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1028995|NM_006015.6(ARID1A):c.3539+5G>A|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1028996|NM_006015.6(ARID1A):c.4792C>T (p.Arg1598Cys)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1028997|NM_006015.6(ARID1A):c.5963T>C (p.Ile1988Thr)|single nucleotide variant|Likely pathogenic|ARID1A|criteria provided, single submitter|1","1031594|NM_006015.6(ARID1A):c.1430A>G (p.His477Arg)|single nucleotide variant|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1031595|NM_006015.6(ARID1A):c.197C>G (p.Pro66Arg)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1031596|NM_006015.6(ARID1A):c.2380G>A (p.Gly794Arg)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1031597|NM_006015.6(ARID1A):c.2630C>T (p.Pro877Leu)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, multiple submitters, no conflicts|1","1031598|NM_006015.6(ARID1A):c.4114C>A (p.Pro1372Thr)|single nucleotide variant|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1031599|NM_006015.6(ARID1A):c.4631C>T (p.Ser1544Leu)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1059864|NM_006015.6(ARID1A):c.5153A>G (p.Glu1718Gly)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1064818|NM_006015.6(ARID1A):c.2149G>A (p.Ala717Thr)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1065491|NM_006015.6(ARID1A):c.175G>T (p.Glu59Ter)|single nucleotide variant|Pathogenic|ARID1A|criteria provided, single submitter|1","1082871|NM_006015.6(ARID1A):c.4724C>A (p.Pro1575Gln)|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1098604|NM_006015.6(ARID1A):c.764C>T (p.Ser255Phe)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1098617|NM_006015.6(ARID1A):c.2194C>A (p.Gln732Lys)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, multiple submitters, no conflicts|1","1098623|NM_006015.6(ARID1A):c.122C>T (p.Ala41Val)|single nucleotide variant|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1120179|NM_006015.6(ARID1A):c.5940_6000del (p.Val1982fs)|Deletion|Pathogenic|ARID1A|criteria provided, single submitter|1","1172645|NM_006015.6(ARID1A):c.4049del (p.Ser1350fs)|Deletion|Likely pathogenic|ARID1A|criteria provided, single submitter|1","1173044|NM_006015.6(ARID1A):c.1803+5G>C|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1174762|NM_006015.6(ARID1A):c.2870A>G (p.Asn957Ser)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, multiple submitters, no conflicts|1","1175604|NM_006015.6(ARID1A):c.759C>G (p.Pro253=)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1176187|NM_006015.6(ARID1A):c.480C>T (p.Ala160=)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1176188|NM_006015.6(ARID1A):c.3169T>C (p.Ser1057Pro)|single nucleotide variant|Likely pathogenic|ARID1A|criteria provided, multiple submitters, no conflicts|1","1177329|NM_006015.6(ARID1A):c.166C>T (p.Gln56Ter)|single nucleotide variant|Pathogenic|ARID1A|criteria provided, multiple submitters, no conflicts|1","1177330|NM_006015.6(ARID1A):c.1708_1766del (p.Pro570fs)|Deletion|Pathogenic|ARID1A|criteria provided, single submitter|1","1177343|NM_006015.6(ARID1A):c.2914del (p.Asp972fs)|Deletion|Pathogenic|ARID1A|criteria provided, single submitter|1","1177344|NM_006015.6(ARID1A):c.3146T>G (p.Leu1049Arg)|single nucleotide variant|Likely pathogenic|ARID1A|criteria provided, single submitter|1","1177345|NM_006015.6(ARID1A):c.6490C>T (p.Arg2164Trp)|single nucleotide variant|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1181346|NM_006015.6(ARID1A):c.456A>G (p.Gln152=)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1182296|NM_006015.6(ARID1A):c.3230C>A (p.Ala1077Glu)|single nucleotide variant|Pathogenic/Likely pathogenic|ARID1A|criteria provided, multiple submitters, no conflicts|1","1183815|NM_006015.6(ARID1A):c.2298G>A (p.Gln766=)|single nucleotide variant|Benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1184821|GRCh37/hg19 1p36.11(chr1:27001498-27110331)x3|copy number gain|Likely pathogenic|ARID1A|no assertion criteria provided|1","1186601|NM_006015.6(ARID1A):c.2733-290A>G|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1186769|NM_006015.6(ARID1A):c.405T>G (p.Pro135=)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1187443|NM_006015.6(ARID1A):c.6070C>T (p.Arg2024Trp)|single nucleotide variant|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1190267|NM_006015.6(ARID1A):c.2881A>C (p.Met961Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1191666|NM_006015.6(ARID1A):c.3199-216dup|Duplication|Likely benign|ARID1A|criteria provided, single submitter|1","1191669|NM_006015.6(ARID1A):c.6582C>T (p.Asn2194=)|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1192736|NM_006015.6(ARID1A):c.*5C>T|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1193038|NM_006015.6(ARID1A):c.6709G>A (p.Ala2237Thr)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1193562|NM_006015.6(ARID1A):c.2732+160G>A|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1194135|NM_006015.6(ARID1A):c.1292C>T (p.Pro431Leu)|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1194854|NM_006015.6(ARID1A):c.4947A>G (p.Thr1649=)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1195455|NM_006015.6(ARID1A):c.2229A>G (p.Gln743=)|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1195523|NM_006015.6(ARID1A):c.591G>T (p.Gly197=)|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1195536|NM_006015.6(ARID1A):c.927G>A (p.Gln309=)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1196223|NM_006015.6(ARID1A):c.3199-25C>T|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1196385|NM_006015.6(ARID1A):c.482T>C (p.Val161Ala)|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1196386|NM_006015.6(ARID1A):c.2657C>T (p.Pro886Leu)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, multiple submitters, no conflicts|1","1196466|NM_006015.6(ARID1A):c.4576G>A (p.Val1526Met)|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1197106|NM_006015.6(ARID1A):c.*10G>T|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1197290|NM_006015.6(ARID1A):c.1350+25G>C|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1197534|NM_006015.6(ARID1A):c.6807A>G (p.Ser2269=)|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1197625|NM_006015.6(ARID1A):c.376G>A (p.Gly126Ser)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1199020|NM_006015.6(ARID1A):c.4993+22G>C|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1199835|NM_006015.6(ARID1A):c.2T>C (p.Met1Thr)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1203777|NM_006015.6(ARID1A):c.2698G>A (p.Ala900Thr)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1203819|NM_006015.6(ARID1A):c.6730G>T (p.Val2244Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1204764|NM_006015.6(ARID1A):c.4564G>A (p.Ala1522Thr)|single nucleotide variant|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1205023|NM_006015.6(ARID1A):c.261_278del (p.Ala88_Gly93del)|Deletion|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1205794|NM_006015.6(ARID1A):c.2668A>G (p.Met890Val)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1206070|NM_006015.6(ARID1A):c.3716-7C>T|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1207173|NM_006015.6(ARID1A):c.1803+274TTTTA[6]|Microsatellite|Likely benign|ARID1A|criteria provided, single submitter|1","1207321|NM_006015.6(ARID1A):c.6708C>T (p.Arg2236=)|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1207976|NM_006015.6(ARID1A):c.3199-74G>C|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1208733|NM_006015.6(ARID1A):c.3978G>A (p.Pro1326=)|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1209320|NM_006015.6(ARID1A):c.3716-149C>A|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1211197|NM_006015.6(ARID1A):c.372C>T (p.Gly124=)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1211215|NM_006015.6(ARID1A):c.4004+35C>T|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1211592|NM_006015.6(ARID1A):c.375T>C (p.Gly125=)|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1211712|NC_000001.11:g.26695829G>A|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1212594|NM_006015.6(ARID1A):c.865C>T (p.Pro289Ser)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1212747|NM_006015.6(ARID1A):c.6331G>A (p.Val2111Ile)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1213731|NM_006015.6(ARID1A):c.269G>C (p.Ser90Thr)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1213757|NM_006015.6(ARID1A):c.1517C>G (p.Ser506Cys)|single nucleotide variant|Uncertain significance|ARID1A|criteria provided, single submitter|1","1214712|NM_006015.6(ARID1A):c.*37C>G|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1216141|NM_006015.6(ARID1A):c.263_277del (p.Ala88_Gly92del)|Deletion|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1216595|NM_006015.6(ARID1A):c.2419+298del|Deletion|Likely benign|ARID1A|criteria provided, single submitter|1","1217160|NM_006015.6(ARID1A):c.5449G>A (p.Val1817Ile)|single nucleotide variant|Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1219322|NC_000001.11:g.26695894T>C|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1219803|NM_006015.6(ARID1A):c.5124+123C>G|single nucleotide variant|Likely benign|ARID1A|criteria provided, single submitter|1","1223603|NM_006015.6(ARID1A):c.437C>T (p.Pro146Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|ARID1A|criteria provided, conflicting classifications|1","1225856|NM_006015.6(ARID1A):c.4563C>T (p.Pro1521=)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1226242|NM_006015.6(ARID1A):c.-27C>T|single nucleotide variant|Benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1226646|NM_006015.6(ARID1A):c.1920+51A>C|single nucleotide variant|Benign|ARID1A|criteria provided, single submitter|1","1226881|NM_006015.6(ARID1A):c.*25C>T|single nucleotide variant|Benign|ARID1A|criteria provided, single submitter|1","1228712|NM_006015.6(ARID1A):c.5287GAA[4] (p.Glu1767del)|Microsatellite|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1229299|NM_006015.6(ARID1A):c.4779G>T (p.Arg1593=)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1230604|NM_006015.6(ARID1A):c.2252-97A>T|single nucleotide variant|Benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1232241|NM_006015.6(ARID1A):c.1266C>T (p.Tyr422=)|single nucleotide variant|Benign/Likely benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1237705|NM_006015.6(ARID1A):c.4994-20G>C|single nucleotide variant|Benign|ARID1A|criteria provided, multiple submitters, no conflicts|1","1240963|NM_006015.6(ARID1A):c.1920+51A>G|single nucleotide variant|Benign|ARID1A|criteria provided, multiple submitters, no conflicts|1"]}]}