{"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:2928,10,HGNC:2928,91,1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:2928","source":"HGNC:2928|dystrophin","targets":["1000393|NM_004006.3(DMD):c.5468C>G (p.Thr1823Ser)|single nucleotide variant|Likely benign|DMD|criteria provided, single submitter|X","1001377|NM_004006.3(DMD):c.11018G>A (p.Arg3673Lys)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1001446|NM_004006.3(DMD):c.2462A>G (p.Glu821Gly)|single nucleotide variant|Likely benign|DMD|criteria provided, single submitter|X","1001786|NM_004006.3(DMD):c.2400C>A (p.Ser800Arg)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1001994|NM_004006.3(DMD):c.2090A>G (p.Lys697Arg)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1002425|NM_004006.3(DMD):c.5154+8A>G|single nucleotide variant|Likely benign|DMD|criteria provided, single submitter|X","1002534|NM_004006.3(DMD):c.2384G>T (p.Gly795Val)|single nucleotide variant|Likely benign|DMD|criteria provided, multiple submitters, no conflicts|X","1002679|NM_004006.3(DMD):c.399A>T (p.Gln133His)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1003362|NM_004006.3(DMD):c.10951G>A (p.Asp3651Asn)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1003542|NM_004006.3(DMD):c.5684A>T (p.Asp1895Val)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1003654|NM_004006.3(DMD):c.6704G>C (p.Ser2235Thr)|single nucleotide variant|Likely benign|DMD|criteria provided, multiple submitters, no conflicts|X","1003749|NC_000023.10:g.(?_31514895)_(32430040_?)dup|Duplication|Uncertain significance|DMD|criteria provided, single submitter|X","1003878|NM_004006.3(DMD):c.961-4del|Deletion|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1004244|NM_004006.3(DMD):c.2354A>G (p.Gln785Arg)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1004386|NM_004006.3(DMD):c.4739T>G (p.Met1580Arg)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1004607|NM_004006.3(DMD):c.80C>T (p.Ala27Val)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1004650|NM_004006.3(DMD):c.4705T>C (p.Cys1569Arg)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1005366|NM_004006.3(DMD):c.2421A>C (p.Gln807His)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1007178|NM_004006.3(DMD):c.6557G>A (p.Gly2186Glu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1007388|NM_004006.3(DMD):c.3134A>T (p.Glu1045Val)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1007599|NM_004006.3(DMD):c.7015C>A (p.His2339Asn)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1007644|NM_004006.3(DMD):c.3806A>C (p.His1269Pro)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1007648|NM_004006.3(DMD):c.5615C>A (p.Ala1872Asp)|single nucleotide variant|Likely benign|DMD|criteria provided, single submitter|X","1007740|NM_004006.3(DMD):c.6238C>A (p.Gln2080Lys)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1008130|NM_004006.3(DMD):c.612A>G (p.Arg204=)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1008232|NM_004006.3(DMD):c.2130G>T (p.Lys710Asn)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1008360|NM_004006.3(DMD):c.8999G>T (p.Arg3000Leu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1008372|NM_004006.3(DMD):c.4190T>C (p.Ile1397Thr)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1008446|NM_004006.3(DMD):c.2866CAG[1] (p.Gln957del)|Microsatellite|Uncertain significance|DMD|criteria provided, single submitter|X","1009457|NM_004006.3(DMD):c.2776C>A (p.Gln926Lys)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1009830|NM_004006.3(DMD):c.139G>A (p.Gly47Arg)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1010272|NM_004006.3(DMD):c.1026C>G (p.Asp342Glu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1010925|NM_004006.3(DMD):c.5195A>G (p.Asp1732Gly)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1011065|NM_004006.3(DMD):c.2150A>T (p.Asp717Val)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1011101|NM_004006.3(DMD):c.7981A>G (p.Met2661Val)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1011748|NM_004006.3(DMD):c.8581G>A (p.Val2861Ile)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1011777|NM_004006.3(DMD):c.6329A>G (p.His2110Arg)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1012103|NM_004006.3(DMD):c.3069A>C (p.Glu1023Asp)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1012643|NM_004006.3(DMD):c.5190G>T (p.Lys1730Asn)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1012645|NM_004006.3(DMD):c.649G>A (p.Asp217Asn)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1012902|GRCh37/hg19 Xp21.1(chrX:32235033-32235180)x4|copy number gain|Pathogenic|DMD|criteria provided, single submitter|X","1014174|NM_004006.3(DMD):c.8018T>G (p.Ile2673Ser)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1014310|NM_004006.3(DMD):c.4143A>T (p.Leu1381Phe)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1014510|NM_004006.3(DMD):c.6398C>A (p.Pro2133His)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1014554|NM_004006.3(DMD):c.4660G>A (p.Glu1554Lys)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1014878|NM_004006.3(DMD):c.2846G>C (p.Ser949Thr)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1014989|NM_004006.3(DMD):c.4769C>T (p.Thr1590Ile)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1015076|NM_004006.3(DMD):c.881C>T (p.Pro294Leu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1015517|NM_004006.3(DMD):c.7064A>G (p.Asn2355Ser)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1015595|NM_004006.3(DMD):c.5336C>G (p.Pro1779Arg)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1015646|NM_004006.3(DMD):c.8866A>C (p.Ile2956Leu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1015828|NM_004006.3(DMD):c.2732T>C (p.Phe911Ser)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1016566|NM_004006.3(DMD):c.5969C>T (p.Pro1990Leu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1017053|NM_004006.3(DMD):c.8702C>A (p.Thr2901Asn)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1017962|NM_004006.3(DMD):c.1388G>T (p.Trp463Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1018171|NM_004006.3(DMD):c.3677C>G (p.Ala1226Gly)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1018542|NM_004006.3(DMD):c.5684A>G (p.Asp1895Gly)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1019121|NM_004006.3(DMD):c.4765G>A (p.Ala1589Thr)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1019157|NM_004006.3(DMD):c.2957A>G (p.Gln986Arg)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1019814|NM_004006.3(DMD):c.5427G>C (p.Glu1809Asp)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1019815|NM_004006.3(DMD):c.1236A>T (p.Leu412Phe)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1021267|NM_004006.3(DMD):c.9812A>G (p.Asn3271Ser)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1021586|NM_004006.3(DMD):c.8315C>A (p.Ala2772Glu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1021763|NM_004006.3(DMD):c.6886A>G (p.Lys2296Glu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1022418|NM_004006.3(DMD):c.3311G>C (p.Ser1104Thr)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1022596|NM_004006.3(DMD):c.8254T>C (p.Tyr2752His)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1022742|NM_004006.3(DMD):c.326G>C (p.Gly109Ala)|single nucleotide variant|Likely benign|DMD|criteria provided, single submitter|X","1022971|NM_004006.3(DMD):c.3967A>T (p.Ile1323Phe)|single nucleotide variant|Likely benign|DMD|criteria provided, single submitter|X","1022986|NM_004006.3(DMD):c.4945G>T (p.Val1649Leu)|single nucleotide variant|Likely benign|DMD|criteria provided, single submitter|X","1023293|NM_004006.3(DMD):c.3326A>G (p.Asn1109Ser)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1023325|NM_004006.3(DMD):c.2801C>A (p.Thr934Lys)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1023726|NM_004006.3(DMD):c.5557C>G (p.Leu1853Val)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1024098|NM_004006.3(DMD):c.1225A>G (p.Thr409Ala)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1024200|NM_004006.3(DMD):c.6083T>C (p.Phe2028Ser)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1024444|NM_004006.3(DMD):c.818A>T (p.His273Leu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1024486|NC_000023.10:g.(?_32398617)_(32398808_?)dup|Duplication|Uncertain significance|DMD|criteria provided, single submitter|X","1024489|NC_000023.10:g.(?_31947703)_(32381085_?)dup|Duplication|Uncertain significance|DMD|criteria provided, single submitter|X","1024495|NM_004006.3(DMD):c.2761G>A (p.Val921Ile)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1024683|NM_004006.3(DMD):c.3175A>G (p.Thr1059Ala)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1024696|NM_004006.3(DMD):c.6305C>G (p.Ser2102Cys)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1024863|NM_004006.3(DMD):c.1274A>G (p.Asn425Ser)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1024928|NM_004006.3(DMD):c.1340G>T (p.Arg447Ile)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1024941|NM_004006.3(DMD):c.4294C>G (p.Gln1432Glu)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1025152|NM_004006.3(DMD):c.2724T>G (p.Asp908Glu)|single nucleotide variant|Likely benign|DMD|criteria provided, single submitter|X","1025249|NM_004006.3(DMD):c.5963A>G (p.Asp1988Gly)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1025312|NM_004006.3(DMD):c.5779A>C (p.Asn1927His)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1025527|NM_004006.3(DMD):c.10576C>T (p.Arg3526Cys)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1025833|NM_004006.3(DMD):c.9140C>T (p.Pro3047Leu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1026030|NM_004006.3(DMD):c.929C>T (p.Ser310Phe)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1026128|NM_004006.3(DMD):c.6712C>G (p.Leu2238Val)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1026150|NM_004006.3(DMD):c.1348A>G (p.Met450Val)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1026634|NM_004006.3(DMD):c.2834A>G (p.Gln945Arg)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1026802|NM_004006.3(DMD):c.5493A>T (p.Gly1831=)|single nucleotide variant|Likely benign|DMD|criteria provided, single submitter|X","1027017|NM_004006.3(DMD):c.1328G>A (p.Ser443Asn)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X","1027173|NM_004006.3(DMD):c.2346A>T (p.Arg782Ser)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1030734|NM_004006.3(DMD):c.10271C>T (p.Ser3424Leu)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1030735|NM_004006.3(DMD):c.4048C>T (p.Arg1350Cys)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1032175|NM_004006.3(DMD):c.1153T>C (p.Tyr385His)|single nucleotide variant|Uncertain significance|DMD|criteria provided, multiple submitters, no conflicts|X","1034457|NM_004006.3(DMD):c.969A>T (p.Glu323Asp)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","1034584|NM_004006.3(DMD):c.5339T>C (p.Leu1780Ser)|single nucleotide variant|Uncertain significance|DMD|criteria provided, single submitter|X"]}]}