{"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:11283,10,HGNC:11283,152,1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:11283","source":"HGNC:11283|SRC proto-oncogene, non-receptor tyrosine kinase","targets":["100851|NM_198291.3(SRC):c.1200C>G (p.Asn400Lys)|single nucleotide variant|Uncertain significance|SRC|no assertion criteria provided|20","1124551|NM_198291.3(SRC):c.875C>A (p.Thr292Asn)|single nucleotide variant|Likely benign|SRC|criteria provided, multiple submitters, no conflicts|20","1182919|NM_198291.3(SRC):c.250+306del|Deletion|Benign|SRC|criteria provided, single submitter|20","1226484|NM_198291.3(SRC):c.250+257T>G|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1235100|NM_198291.3(SRC):c.250+243T>C|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1236716|NM_198291.3(SRC):c.250+219A>G|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1239174|NM_198291.3(SRC):c.250+211A>G|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","12573|NM_198291.3(SRC):c.1591C>T (p.Gln531Ter)|single nucleotide variant|Pathogenic|SRC|no assertion criteria provided|20","1262217|NM_198291.3(SRC):c.250+249T>G|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1262847|NM_198291.3(SRC):c.250+270_250+271insG|Insertion|Benign|SRC|criteria provided, single submitter|20","1266384|NM_198291.3(SRC):c.250+238T>G|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1268247|NM_198291.3(SRC):c.1271-55=|single nucleotide variant|Benign|SRC|criteria provided, multiple submitters, no conflicts|20","1268676|NM_198291.3(SRC):c.250+259A>G|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1269563|NM_198291.3(SRC):c.250+235T>G|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1271503|NM_198291.3(SRC):c.250+237A>T|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1272399|NM_198291.3(SRC):c.1117-180C>T|single nucleotide variant|Benign|SRC|criteria provided, multiple submitters, no conflicts|20","1275298|NM_198291.3(SRC):c.250+265_250+268del|Deletion|Benign|SRC|criteria provided, single submitter|20","1276301|NM_198291.3(SRC):c.250+247A>G|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1281875|NM_198291.3(SRC):c.250+217A>G|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1288138|NM_198291.3(SRC):c.250+223A>G|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","1337115|NM_198291.3(SRC):c.582C>T (p.Phe194=)|single nucleotide variant|Likely benign|SRC|criteria provided, single submitter|20","1337663|NM_198291.3(SRC):c.553+9G>T|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","2234627|NM_198291.3(SRC):c.1018G>A (p.Val340Ile)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","225689|NM_198291.3(SRC):c.1579G>A (p.Glu527Lys)|single nucleotide variant|Likely pathogenic|SRC|criteria provided, single submitter|20","2310404|NM_198291.3(SRC):c.811C>T (p.Arg271Trp)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","2388133|NM_198291.3(SRC):c.475C>T (p.Arg159Trp)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","2475250|NM_198291.3(SRC):c.296C>T (p.Thr99Met)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","2477836|NM_198291.3(SRC):c.327G>T (p.Glu109Asp)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","2548214|NM_198291.3(SRC):c.1439G>A (p.Arg480Gln)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","2572134|NM_198291.3(SRC):c.1585C>G (p.Gln529Glu)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","2584809|NM_198291.3(SRC):c.919C>T (p.Pro307Ser)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","2614414|NM_198291.3(SRC):c.869A>G (p.Asn290Ser)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","2619551|NM_198291.3(SRC):c.890T>C (p.Ile297Thr)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3033317|NM_198291.3(SRC):c.525C>T (p.Phe175=)|single nucleotide variant|Likely benign|SRC|no assertion criteria provided|20","3042787|NM_198291.3(SRC):c.849G>A (p.Glu283=)|single nucleotide variant|Likely benign|SRC|no assertion criteria provided|20","3043475|NM_198291.3(SRC):c.636C>T (p.Ser212=)|single nucleotide variant|Likely benign|SRC|no assertion criteria provided|20","3047023|NM_198291.3(SRC):c.1596C>G (p.Pro532=)|single nucleotide variant|Likely benign|SRC|no assertion criteria provided|20","3050520|NM_198291.3(SRC):c.561C>T (p.Tyr187=)|single nucleotide variant|Likely benign|SRC|no assertion criteria provided|20","3067299|NM_198291.3(SRC):c.423G>A (p.Ala141=)|single nucleotide variant|Likely benign|SRC|criteria provided, single submitter|20","3169832|NM_198291.3(SRC):c.529G>T (p.Val177Leu)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3169833|NM_198291.3(SRC):c.871G>T (p.Gly291Cys)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3252560|NM_198291.3(SRC):c.1250_1253del (p.Asn417fs)|Deletion|Uncertain significance|SRC|criteria provided, single submitter|20","3252895|NM_198291.3(SRC):c.1039+5G>C|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3322569|NM_198291.3(SRC):c.1460C>T (p.Pro487Leu)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3322570|NM_198291.3(SRC):c.1513G>C (p.Glu505Gln)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3352888|NM_198291.3(SRC):c.450-8A>T|single nucleotide variant|Likely benign|SRC|no assertion criteria provided|20","3358112|NM_198291.3(SRC):c.588C>T (p.Asn196=)|single nucleotide variant|Likely benign|SRC|no assertion criteria provided|20","3449216|NM_198291.3(SRC):c.242C>A (p.Pro81Gln)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3449217|NM_198291.3(SRC):c.100G>C (p.Ala34Pro)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3449218|NM_198291.3(SRC):c.797C>T (p.Pro266Leu)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3764601|NM_198291.3(SRC):c.1070C>T (p.Thr357Ile)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3801246|NM_198291.3(SRC):c.871G>A (p.Gly291Ser)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3911454|NM_198291.3(SRC):c.553+8C>T|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","3961842|NM_198291.3(SRC):c.736A>T (p.Thr246Ser)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3961843|NM_198291.3(SRC):c.1486G>A (p.Asp496Asn)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3961844|NM_198291.3(SRC):c.1495T>C (p.Cys499Arg)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","3961845|NM_198291.3(SRC):c.221C>A (p.Thr74Asn)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4174623|NM_198291.3(SRC):c.329G>T (p.Arg110Leu)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4174624|NM_198291.3(SRC):c.1154A>G (p.Tyr385Cys)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4174625|NM_198291.3(SRC):c.1091C>T (p.Pro364Leu)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4174626|NM_198291.3(SRC):c.166C>T (p.Pro56Ser)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4174627|NM_198291.3(SRC):c.1453C>T (p.Pro485Ser)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4174628|NM_198291.3(SRC):c.737C>T (p.Thr246Ile)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4174631|NM_198291.3(SRC):c.799C>T (p.Arg267Trp)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4278080|NM_198291.3(SRC):c.350C>T (p.Thr117Ile)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4450115|NM_198291.3(SRC):c.-5+108G>A|single nucleotide variant||SRC||20","4450117|NM_198291.3(SRC):c.-5+117C>T|single nucleotide variant||SRC||20","4450118|NM_198291.3(SRC):c.-4-3C>T|single nucleotide variant||SRC||20","4450119|NM_198291.3(SRC):c.350+54C>T|single nucleotide variant||SRC||20","4450120|NM_198291.3(SRC):c.436A>C (p.Ile146Leu)|single nucleotide variant||SRC||20","4450121|NM_198291.3(SRC):c.704-1G>A|single nucleotide variant||SRC||20","4450122|NM_198291.3(SRC):c.704-1G>C|single nucleotide variant||SRC||20","4450123|NM_198291.3(SRC):c.831C>T (p.Gly277=)|single nucleotide variant||SRC||20","4450124|NM_198291.3(SRC):c.859+2T>G|single nucleotide variant||SRC||20","4450125|NM_198291.3(SRC):c.1040-12C>G|single nucleotide variant||SRC||20","4450126|NM_198291.3(SRC):c.1367C>G (p.Thr456Ser)|single nucleotide variant||SRC||20","4450127|NM_198291.3(SRC):c.*1863T>A|single nucleotide variant||SRC||20","4450128|NM_198291.3(SRC):c.*1864T>A|single nucleotide variant||SRC||20","4542388|NM_198291.3(SRC):c.739G>A (p.Val247Met)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4589424|NM_198291.3(SRC):c.889A>T (p.Ile297Phe)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4589425|NM_198291.3(SRC):c.884T>A (p.Val295Glu)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4589426|NM_198291.3(SRC):c.164C>T (p.Ala55Val)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4589427|NM_198291.3(SRC):c.1145G>A (p.Arg382Gln)|single nucleotide variant|Uncertain significance|SRC|criteria provided, single submitter|20","4684417|NM_198291.3(SRC):c.135C>T (p.Asp45=)|single nucleotide variant|Likely benign|SRC|criteria provided, single submitter|20","4684418|NM_198291.3(SRC):c.408C>T (p.Pro136=)|single nucleotide variant|Likely benign|SRC|criteria provided, single submitter|20","708134|NM_198291.3(SRC):c.449+9C>T|single nucleotide variant|Benign/Likely benign|SRC|criteria provided, multiple submitters, no conflicts|20","713171|NM_198291.3(SRC):c.1467G>A (p.Glu489=)|single nucleotide variant|Benign/Likely benign|SRC|criteria provided, multiple submitters, no conflicts|20","714817|NM_198291.3(SRC):c.1128C>A (p.Gly376=)|single nucleotide variant|Benign/Likely benign|SRC|criteria provided, multiple submitters, no conflicts|20","714899|NM_198291.3(SRC):c.387A>G (p.Thr129=)|single nucleotide variant|Benign/Likely benign|SRC|criteria provided, multiple submitters, no conflicts|20","719597|NM_198291.3(SRC):c.1254G>A (p.Glu418=)|single nucleotide variant|Benign|SRC|criteria provided, multiple submitters, no conflicts|20","725075|NM_198291.3(SRC):c.1117-9C>T|single nucleotide variant|Likely benign|SRC|criteria provided, multiple submitters, no conflicts|20","727273|NM_198291.3(SRC):c.930C>T (p.Phe310=)|single nucleotide variant|Likely benign|SRC|criteria provided, single submitter|20","734030|NM_198291.3(SRC):c.1224T>C (p.Phe408=)|single nucleotide variant|Benign|SRC|criteria provided, multiple submitters, no conflicts|20","741406|NM_198291.3(SRC):c.1596C>T (p.Pro532=)|single nucleotide variant|Likely benign|SRC|criteria provided, single submitter|20","742883|NM_198291.3(SRC):c.1143G>A (p.Glu381=)|single nucleotide variant|Likely benign|SRC|criteria provided, single submitter|20","747464|NM_198291.3(SRC):c.684G>A (p.Gln228=)|single nucleotide variant|Benign|SRC|criteria provided, single submitter|20","777572|NM_198291.3(SRC):c.554-5C>T|single nucleotide variant|Benign|SRC|criteria provided, multiple submitters, no conflicts|20","777573|NM_198291.3(SRC):c.1134G>A (p.Ala378=)|single nucleotide variant|Benign|SRC|criteria provided, multiple submitters, no conflicts|20","795540|NM_198291.3(SRC):c.429C>T (p.Ser143=)|single nucleotide variant|Likely benign|SRC|criteria provided, single submitter|20","98523|NM_198291.3(SRC):c.12C>T (p.Asn4=)|single nucleotide variant|not provided|SRC|no classification provided|20"]}]}