{"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:3236,10,HGNC:3236,173,3]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:3236","source":"HGNC:3236|epidermal growth factor receptor","targets":["1000076|NM_005228.5(EGFR):c.840C>A (p.Asn280Lys)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1000203|NM_005228.5(EGFR):c.664C>T (p.Arg222Cys)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1000496|NM_005228.5(EGFR):c.494G>A (p.Arg165Gln)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1000546|NM_005228.5(EGFR):c.652C>A (p.Gln218Lys)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1000851|NM_005228.5(EGFR):c.1813A>G (p.Thr605Ala)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1000960|NM_005228.5(EGFR):c.2653T>G (p.Ser885Ala)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1001152|NM_005228.5(EGFR):c.991G>A (p.Gly331Arg)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1001187|NM_005228.5(EGFR):c.1822T>A (p.Trp608Arg)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1001705|NM_005228.5(EGFR):c.1559C>T (p.Pro520Leu)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1001710|NM_005228.5(EGFR):c.2741C>G (p.Pro914Arg)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1001782|NM_005228.5(EGFR):c.2619A>T (p.Gly873=)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1002380|NM_005228.5(EGFR):c.2339T>C (p.Ile780Thr)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1002493|NM_005228.5(EGFR):c.1670A>G (p.Gln557Arg)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1002562|NM_005228.5(EGFR):c.721A>G (p.Thr241Ala)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1002578|NM_005228.5(EGFR):c.3031G>C (p.Val1011Leu)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1002794|NM_005228.5(EGFR):c.3209G>A (p.Ser1070Asn)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1003132|NM_005228.5(EGFR):c.1463C>G (p.Thr488Ser)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1003262|NM_005228.5(EGFR):c.2917C>G (p.Arg973Gly)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1003305|NM_005228.5(EGFR):c.1049C>G (p.Ser350Cys)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1003743|NM_005228.5(EGFR):c.1675C>T (p.His559Tyr)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1003794|NM_005228.5(EGFR):c.1975G>C (p.Val659Leu)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1004032|NM_005228.5(EGFR):c.2833A>G (p.Met945Val)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1004363|NM_005228.5(EGFR):c.541C>G (p.Gln181Glu)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1004409|NM_005228.5(EGFR):c.1739T>C (p.Ile580Thr)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1004521|NM_005228.5(EGFR):c.1582A>G (p.Asn528Asp)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1005378|NM_005228.5(EGFR):c.2161G>A (p.Gly721Ser)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1005727|NM_005228.5(EGFR):c.1605C>A (p.Cys535Ter)|single nucleotide variant|Pathogenic|EGFR|criteria provided, single submitter|7","1005794|NM_005228.5(EGFR):c.3437G>T (p.Cys1146Phe)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1006525|NM_005228.5(EGFR):c.2185-3T>C|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1006618|NM_005228.5(EGFR):c.268C>T (p.Leu90Phe)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1006728|NM_005228.5(EGFR):c.437G>A (p.Gly146Asp)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1007379|NM_005228.5(EGFR):c.3056C>T (p.Pro1019Leu)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1007424|NM_005228.5(EGFR):c.2091A>C (p.Glu697Asp)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1007638|NC_000007.13:g.(?_55086971)_(55087068_?)dup|Duplication|Uncertain significance|EGFR|criteria provided, single submitter|7","1007797|NM_005228.5(EGFR):c.2150T>C (p.Val717Ala)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1008399|NM_005228.5(EGFR):c.3574G>A (p.Ala1192Thr)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1008401|NM_005228.5(EGFR):c.2537A>G (p.Lys846Arg)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1009011|NM_005228.5(EGFR):c.1795G>A (p.Val599Ile)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1009550|NM_005228.5(EGFR):c.3575C>G (p.Ala1192Gly)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1009597|NM_005228.5(EGFR):c.730C>T (p.Arg244Trp)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1009894|NM_005228.5(EGFR):c.3162+1G>T|single nucleotide variant|Likely pathogenic|EGFR|criteria provided, single submitter|7","1009949|NM_005228.5(EGFR):c.1606G>T (p.Val536Leu)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1009989|NM_005228.5(EGFR):c.2947-1G>A|single nucleotide variant|Likely pathogenic|EGFR|criteria provided, single submitter|7","1010048|NM_005228.5(EGFR):c.1748C>T (p.Ala583Val)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1011022|NM_005228.5(EGFR):c.658T>C (p.Ser220Pro)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1011360|NM_005228.5(EGFR):c.1936A>G (p.Ile646Val)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1011404|NM_005228.5(EGFR):c.89T>C (p.Val30Ala)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1012017|NM_005228.5(EGFR):c.3387C>A (p.His1129Gln)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1012132|NM_005228.5(EGFR):c.2299G>T (p.Ala767Ser)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1013692|NM_005228.5(EGFR):c.1693C>G (p.Gln565Glu)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1013771|NM_005228.5(EGFR):c.2918G>A (p.Arg973Gln)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1013792|NM_005228.5(EGFR):c.2858T>G (p.Ile953Arg)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1014020|NM_005228.5(EGFR):c.3073A>G (p.Ser1025Gly)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1014375|NM_005228.5(EGFR):c.547C>A (p.His183Asn)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1014501|NM_005228.5(EGFR):c.2402A>G (p.Tyr801Cys)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1014610|NM_005228.5(EGFR):c.175G>A (p.Glu59Lys)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1014793|NM_005228.5(EGFR):c.2509G>A (p.Asp837Asn)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1015382|NM_005228.5(EGFR):c.2303G>A (p.Ser768Asn)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1015895|NM_005228.5(EGFR):c.257C>T (p.Ala86Val)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1016162|NM_005228.5(EGFR):c.3442A>G (p.Asn1148Asp)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1016241|NM_005228.5(EGFR):c.2917C>T (p.Arg973Ter)|single nucleotide variant|Pathogenic|EGFR|criteria provided, single submitter|7","1016463|NM_005228.5(EGFR):c.1536del (p.Glu513fs)|Deletion|Pathogenic|EGFR|criteria provided, single submitter|7","1016573|NM_005228.5(EGFR):c.1488A>C (p.Glu496Asp)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1016864|NM_005228.5(EGFR):c.3490C>A (p.Gln1164Lys)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1016924|NM_005228.5(EGFR):c.3110C>T (p.Ser1037Phe)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1017030|NM_005228.5(EGFR):c.2909A>G (p.Lys970Arg)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1017073|NM_005228.5(EGFR):c.3506A>G (p.Asn1169Ser)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1017568|NM_005228.5(EGFR):c.1061C>T (p.Thr354Met)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1017706|NM_005228.5(EGFR):c.8C>T (p.Pro3Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1017797|NM_005228.5(EGFR):c.3114G>A (p.Leu1038=)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1018033|NM_005228.5(EGFR):c.3566G>A (p.Gly1189Asp)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1018297|NM_005228.5(EGFR):c.2682G>C (p.Gln894His)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1018424|NM_005228.5(EGFR):c.946T>A (p.Tyr316Asn)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1018440|NM_005228.5(EGFR):c.388A>G (p.Thr130Ala)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1018590|NM_005228.5(EGFR):c.2836A>G (p.Ile946Val)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1018687|NM_005228.5(EGFR):c.1351C>T (p.Arg451Cys)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1018719|NM_005228.5(EGFR):c.615G>C (p.Glu205Asp)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1018840|NM_005228.5(EGFR):c.925C>T (p.Arg309Ter)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1018921|NM_005228.5(EGFR):c.2267A>G (p.Asn756Ser)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1019264|NM_005228.5(EGFR):c.1001G>A (p.Arg334His)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1019294|NM_005228.5(EGFR):c.3215A>G (p.Asp1072Gly)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1019301|NM_005228.5(EGFR):c.2336G>A (p.Gly779Asp)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1019405|NM_005228.5(EGFR):c.715G>A (p.Gly239Ser)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1019778|NM_005228.5(EGFR):c.3052A>G (p.Ile1018Val)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1019807|NM_005228.5(EGFR):c.628+6T>A|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1019826|NM_005228.5(EGFR):c.1499-4G>T|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1020012|NM_005228.5(EGFR):c.3244A>T (p.Ile1082Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1020225|NM_005228.5(EGFR):c.1960C>T (p.Leu654Phe)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1020266|NC_000007.13:g.(?_55209969)_(55223649_?)del|Deletion|Uncertain significance|EGFR|criteria provided, single submitter|7","1020327|NM_005228.5(EGFR):c.514T>C (p.Phe172Leu)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1020474|NM_005228.5(EGFR):c.1937T>G (p.Ile646Ser)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1020563|NM_005228.5(EGFR):c.2533G>C (p.Val845Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1020888|NM_005228.5(EGFR):c.1579C>G (p.Arg527Gly)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1021051|NM_005228.5(EGFR):c.3529T>C (p.Phe1177Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1021163|NM_005228.5(EGFR):c.431T>C (p.Leu144Pro)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1021254|NM_005228.5(EGFR):c.2006G>A (p.Arg669Gln)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1021477|NM_005228.5(EGFR):c.3571A>G (p.Thr1191Ala)|single nucleotide variant|Conflicting classifications of pathogenicity|EGFR|criteria provided, conflicting classifications|7","1022110|NM_005228.5(EGFR):c.241A>G (p.Thr81Ala)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7","1022124|NM_005228.5(EGFR):c.1836C>A (p.Asp612Glu)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, single submitter|7","1022337|NM_005228.5(EGFR):c.3237G>C (p.Glu1079Asp)|single nucleotide variant|Uncertain significance|EGFR|criteria provided, multiple submitters, no conflicts|7"]}]}