{"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:795,10,HGNC:795,44,2]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:795","source":"HGNC:795|ATM serine/threonine kinase","targets":["1000108|NM_000051.4(ATM):c.7743C>A (p.Ser2581Arg)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1000182|NM_000051.4(ATM):c.7964A>C (p.Lys2655Thr)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1000339|NM_000051.4(ATM):c.25C>T (p.Leu9Phe)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1000362|NM_000051.4(ATM):c.326A>G (p.Asn109Ser)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1000438|NM_000051.4(ATM):c.3095G>A (p.Arg1032Lys)|single nucleotide variant|Conflicting classifications of pathogenicity|ATM|criteria provided, conflicting classifications|11","1000441|NM_000051.4(ATM):c.3920G>A (p.Gly1307Glu)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1000615|NM_000051.4(ATM):c.2611G>C (p.Glu871Gln)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1000625|NM_000051.4(ATM):c.7346A>G (p.Glu2449Gly)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1000637|NM_000051.4(ATM):c.2922-10T>G|single nucleotide variant|Likely benign|ATM|criteria provided, single submitter|11","1000639|NM_000051.4(ATM):c.6169T>C (p.Ser2057Pro)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1000731|NM_000051.4(ATM):c.6667A>C (p.Ile2223Leu)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1000876|NM_000051.4(ATM):c.1043T>C (p.Leu348Ser)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1001071|NM_000051.4(ATM):c.52G>A (p.Asp18Asn)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1001330|NM_000051.4(ATM):c.1147C>G (p.Pro383Ala)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1001363|NM_000051.4(ATM):c.8077G>A (p.Ala2693Thr)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1001382|NM_000051.4(ATM):c.567A>T (p.Arg189Ser)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1001474|NM_000051.4(ATM):c.5913G>T (p.Glu1971Asp)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1001554|NM_000051.4(ATM):c.8105T>C (p.Ile2702Thr)|single nucleotide variant|Conflicting classifications of pathogenicity|ATM|criteria provided, conflicting classifications|11","1001572|NM_000051.4(ATM):c.1981G>C (p.Asp661His)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1001599|NM_000051.4(ATM):c.9171A>T (p.Ter3057Cys)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1001695|NM_000051.4(ATM):c.4673C>A (p.Thr1558Lys)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1001777|NM_000051.4(ATM):c.1301C>T (p.Pro434Leu)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1001835|NM_000051.4(ATM):c.8269-7A>G|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1002463|NM_000051.4(ATM):c.2715T>G (p.Cys905Trp)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1002472|NM_000051.4(ATM):c.673A>C (p.Ser225Arg)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1002477|NM_000051.4(ATM):c.6070G>T (p.Gly2024Trp)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1002705|NM_000051.4(ATM):c.6751C>G (p.Leu2251Val)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1002715|NM_000051.4(ATM):c.7123A>G (p.Ser2375Gly)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1002951|NM_000051.4(ATM):c.4110-10A>G|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1003002|NM_000051.4(ATM):c.2467-9T>A|single nucleotide variant|Likely benign|ATM|criteria provided, single submitter|11","1003314|NM_000051.4(ATM):c.3803T>C (p.Val1268Ala)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1003616|NM_000051.4(ATM):c.804A>G (p.Gln268=)|single nucleotide variant|Benign/Likely benign|ATM|criteria provided, multiple submitters, no conflicts|11","1003628|NM_000051.4(ATM):c.143A>G (p.Asp48Gly)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1003631|NM_000051.4(ATM):c.2608A>C (p.Asn870His)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1003724|NM_000051.4(ATM):c.2648A>G (p.Asn883Ser)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1003804|NM_000051.4(ATM):c.6878T>C (p.Leu2293Pro)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1004128|NM_000051.4(ATM):c.1494G>C (p.Glu498Asp)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1004132|NM_000051.4(ATM):c.5426T>A (p.Leu1809Gln)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1004365|NM_000051.4(ATM):c.2098C>G (p.Gln700Glu)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1004438|NM_000051.4(ATM):c.5401A>T (p.Asn1801Tyr)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1004996|NM_000051.4(ATM):c.4143T>G (p.Phe1381Leu)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1005169|NM_000051.4(ATM):c.8777T>G (p.Val2926Gly)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1005285|NM_000051.4(ATM):c.6857G>T (p.Cys2286Phe)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1005372|NM_000051.4(ATM):c.992A>T (p.Lys331Met)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1005729|NM_000051.4(ATM):c.5615G>A (p.Ser1872Asn)|single nucleotide variant|Conflicting classifications of pathogenicity|ATM|criteria provided, conflicting classifications|11","1005823|NM_000051.4(ATM):c.901G>C (p.Gly301Arg)|single nucleotide variant|Conflicting classifications of pathogenicity|ATM|criteria provided, conflicting classifications|11","1005916|NM_000051.4(ATM):c.2409C>G (p.Phe803Leu)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1006125|NM_000051.4(ATM):c.5990C>T (p.Thr1997Ile)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1006369|NM_000051.4(ATM):c.2885C>G (p.Pro962Arg)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1006532|NM_000051.4(ATM):c.3239A>G (p.Asp1080Gly)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1006533|NM_000051.4(ATM):c.565A>G (p.Arg189Gly)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1006630|NM_000051.4(ATM):c.2639-7T>G|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1006762|NM_000051.4(ATM):c.544G>A (p.Val182Ile)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1006967|NM_000051.4(ATM):c.3457G>A (p.Val1153Ile)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1007070|NM_000051.4(ATM):c.4436+6T>C|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1007092|NM_000051.4(ATM):c.5031A>C (p.Glu1677Asp)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1007185|NM_000051.4(ATM):c.2014G>C (p.Glu672Gln)|single nucleotide variant|Conflicting classifications of pathogenicity|ATM|criteria provided, conflicting classifications|11","1007298|NM_000051.4(ATM):c.1533A>G (p.Ile511Met)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1007387|NM_000051.4(ATM):c.4047G>A (p.Met1349Ile)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1007468|NM_000051.4(ATM):c.3511C>G (p.Gln1171Glu)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1007499|NM_000051.4(ATM):c.8190G>C (p.Gln2730His)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1007530|NM_000051.4(ATM):c.4196C>T (p.Thr1399Ile)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1007724|NM_000051.4(ATM):c.1607+3A>G|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1007824|NM_000051.4(ATM):c.7855A>G (p.Ser2619Gly)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1007926|NM_000051.4(ATM):c.7320G>T (p.Lys2440Asn)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1008115|NM_000051.4(ATM):c.5074A>G (p.Lys1692Glu)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1008171|NM_000051.4(ATM):c.3100T>C (p.Tyr1034His)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1008300|NM_000051.4(ATM):c.8268+4A>G|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1008339|NM_000051.4(ATM):c.308A>G (p.Tyr103Cys)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1008411|NM_000051.4(ATM):c.523T>A (p.Tyr175Asn)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1008502|NM_000051.4(ATM):c.2504T>A (p.Val835Glu)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1008710|NM_000051.4(ATM):c.8735G>C (p.Arg2912Thr)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1008982|NM_000051.4(ATM):c.403G>T (p.Ala135Ser)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1009088|NM_000051.4(ATM):c.4045A>G (p.Met1349Val)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1009106|NM_000051.4(ATM):c.6333_6341dup (p.Ser2114_Val2115insCysThrSer)|Duplication|Uncertain significance|ATM|criteria provided, single submitter|11","1009116|NM_000051.4(ATM):c.7320G>C (p.Lys2440Asn)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1009321|NM_000051.4(ATM):c.3707T>C (p.Phe1236Ser)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1009645|NM_000051.4(ATM):c.663-3C>T|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1009706|NM_000051.4(ATM):c.1608T>C (p.Cys536=)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1009775|NM_000051.4(ATM):c.6781C>G (p.Leu2261Val)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1009833|NM_000051.4(ATM):c.2750C>G (p.Ser917Cys)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1009840|NM_000051.4(ATM):c.6763C>T (p.Leu2255Phe)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1009855|NM_000051.4(ATM):c.5597T>G (p.Val1866Gly)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1010202|NM_000051.4(ATM):c.2378A>G (p.Lys793Arg)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1010286|NM_000051.4(ATM):c.4421A>G (p.His1474Arg)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1010430|NM_000051.4(ATM):c.4723C>G (p.Arg1575Gly)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1010644|NM_000051.4(ATM):c.7977AGA[1] (p.Glu2660del)|Microsatellite|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1010787|NM_000051.4(ATM):c.8919G>T (p.Arg2973Ser)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1010842|NM_000051.4(ATM):c.8600G>A (p.Gly2867Glu)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1011029|NM_000051.4(ATM):c.1633G>C (p.Ala545Pro)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1011173|NM_000051.4(ATM):c.8258G>A (p.Cys2753Tyr)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1011230|NM_000051.4(ATM):c.1487_1489del (p.Ser496_Ser497delinsThr)|Deletion|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1011478|NM_000051.4(ATM):c.2226G>C (p.Lys742Asn)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1011685|NM_000051.4(ATM):c.7537A>G (p.Thr2513Ala)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","1011809|NM_000051.4(ATM):c.3657G>C (p.Leu1219Phe)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1011928|NM_000051.4(ATM):c.8791T>C (p.Cys2931Arg)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1013661|NM_000051.4(ATM):c.4915C>T (p.Pro1639Ser)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1013733|NM_000051.4(ATM):c.3248A>G (p.His1083Arg)|single nucleotide variant|Pathogenic/Likely pathogenic|ATM|criteria provided, multiple submitters, no conflicts|11","1013793|NM_000051.4(ATM):c.4435A>G (p.Arg1479Gly)|single nucleotide variant|Uncertain significance|ATM|criteria provided, single submitter|11","1013913|NM_000051.4(ATM):c.2947G>T (p.Asp983Tyr)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11"]}]}