{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely benign\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HGNC:9884,10,HGNC:9884,93,3]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:9884","source":"HGNC:9884|RB transcriptional corepressor 1","targets":["1037255|NM_000321.3(RB1):c.2602C&gt;A (p.Pro868Thr)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1063131|NM_000321.3(RB1):c.1390-10T&gt;C|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1078753|NM_000321.3(RB1):c.862-9C&gt;T|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1080096|NM_000321.3(RB1):c.1971A&gt;G (p.Leu657=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1080164|NM_000321.3(RB1):c.1284G&gt;A (p.Glu428=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1080700|NM_000321.3(RB1):c.2406G&gt;C (p.Gly802=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1081187|NM_000321.3(RB1):c.1356G&gt;A (p.Leu452=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1081885|NM_000321.3(RB1):c.21A&gt;G (p.Arg7=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1082139|NM_000321.3(RB1):c.2663+10A&gt;G|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1082896|NM_000321.3(RB1):c.876T&gt;C (p.Tyr292=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1083163|NM_000321.3(RB1):c.1962G&gt;T (p.Val654=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1085956|NM_000321.3(RB1):c.849T&gt;C (p.Cys283=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1086306|NM_000321.3(RB1):c.486C&gt;T (p.Phe162=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1087739|NM_000321.3(RB1):c.2046C&gt;T (p.Thr682=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1088803|NM_000321.3(RB1):c.1317C&gt;T (p.Val439=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1091485|NM_000321.3(RB1):c.1233A&gt;G (p.Pro411=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1091948|NM_000321.3(RB1):c.978T&gt;G (p.Leu326=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1092040|NM_000321.3(RB1):c.1499-10T&gt;C|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1093406|NM_000321.3(RB1):c.1944A&gt;G (p.Ser648=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1093556|NM_000321.3(RB1):c.1836T&gt;G (p.Ser612=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1093825|NM_000321.3(RB1):c.2625A&gt;G (p.Leu875=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1094733|NM_000321.3(RB1):c.921A&gt;G (p.Thr307=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1094775|NM_000321.3(RB1):c.1960+8G&gt;T|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1095378|NM_000321.3(RB1):c.2565C&gt;T (p.Ser855=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1095397|NM_000321.3(RB1):c.2685C&gt;G (p.Ser895=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1095655|NM_000321.3(RB1):c.1323T&gt;C (p.Ile441=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1096267|NM_000321.3(RB1):c.2319C&gt;T (p.Ser773=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1097581|NM_000321.3(RB1):c.1308G&gt;A (p.Gln436=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1097686|NM_000321.3(RB1):c.2310G&gt;A (p.Gln770=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1098943|NM_000321.3(RB1):c.396T&gt;C (p.Phe132=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1100379|NM_000321.3(RB1):c.1335A&gt;T (p.Arg445=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1100863|NM_000321.3(RB1):c.1206C&gt;A (p.Ser402=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1103735|NM_000321.3(RB1):c.2394G&gt;T (p.Arg798=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1103913|NM_000321.3(RB1):c.2614C&gt;T (p.Leu872=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1105264|NM_000321.3(RB1):c.1101T&gt;C (p.Asn367=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1105728|NM_000321.3(RB1):c.2082C&gt;T (p.Leu694=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1105927|NM_000321.3(RB1):c.402A&gt;G (p.Leu134=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1106256|NM_000321.3(RB1):c.1311T&gt;C (p.Gly437=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1106945|NM_000321.3(RB1):c.201A&gt;C (p.Pro67=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1107358|NM_000321.3(RB1):c.718+7A&gt;G|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1110110|NM_000321.3(RB1):c.540-5A&gt;C|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1111470|NM_000321.3(RB1):c.363G&gt;A (p.Gln121=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1111751|NM_000321.3(RB1):c.1050-9_1050-7del|Deletion|Likely benign|RB1|criteria provided, single submitter|13","1111839|NM_000321.3(RB1):c.1696-7C&gt;T|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1112019|NM_000321.3(RB1):c.1422-6del|Deletion|Likely benign|RB1|criteria provided, single submitter|13","1112875|NM_000321.3(RB1):c.480A&gt;G (p.Ala160=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1113532|NM_000321.3(RB1):c.1731G&gt;A (p.Lys577=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1113993|NM_000321.3(RB1):c.2490-10A&gt;C|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1114197|NM_000321.3(RB1):c.2694G&gt;A (p.Gln898=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1115171|NM_000321.3(RB1):c.1498+7T&gt;G|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1116318|NM_000321.3(RB1):c.1041T&gt;A (p.Ser347=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1116352|NM_000321.3(RB1):c.501-8C&gt;A|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1116946|NM_000321.3(RB1):c.1110T&gt;G (p.Pro370=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1117822|NM_000321.3(RB1):c.2212-8T&gt;C|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1118480|NM_000321.3(RB1):c.2049T&gt;G (p.Leu683=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1118752|NM_000321.3(RB1):c.1421+11dup|Duplication|Likely benign|RB1|criteria provided, single submitter|13","1119142|NM_000321.3(RB1):c.1221C&gt;T (p.Cys407=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1119440|NM_000321.3(RB1):c.2481A&gt;G (p.Pro827=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1119870|NM_000321.3(RB1):c.609G&gt;A (p.Gly203=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1120754|NM_000321.3(RB1):c.1498+10A&gt;C|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1121475|NM_000321.3(RB1):c.2326-8T&gt;G|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1121924|NM_000321.3(RB1):c.495G&gt;A (p.Leu165=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1122182|NM_000321.3(RB1):c.948T&gt;C (p.Asn316=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1122704|NM_000321.3(RB1):c.1422-10T&gt;C|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1123270|NM_000321.3(RB1):c.2714-4C&gt;T|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1125533|NM_000321.3(RB1):c.852T&gt;C (p.Asn284=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1125676|NM_000321.3(RB1):c.279A&gt;G (p.Gln93=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1127024|NM_000321.3(RB1):c.1980C&gt;G (p.Leu660=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1127072|NM_000321.3(RB1):c.1761A&gt;G (p.Glu587=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1127940|NM_000321.3(RB1):c.138-6T&gt;C|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1128174|NM_000321.3(RB1):c.954T&gt;C (p.Ser318=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1128229|NM_000321.3(RB1):c.1542C&gt;T (p.Phe514=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1128497|NM_000321.3(RB1):c.2623C&gt;T (p.Leu875=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1129133|NM_000321.3(RB1):c.321A&gt;C (p.Ala107=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1130272|NM_000321.3(RB1):c.2472A&gt;G (p.Lys824=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1130288|NM_000321.3(RB1):c.687C&gt;T (p.Leu229=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1130777|NM_000321.3(RB1):c.756A&gt;G (p.Thr252=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1131142|NM_000321.3(RB1):c.2658T&gt;C (p.Asp886=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1133785|NM_000321.3(RB1):c.1499-8A&gt;G|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1133824|NM_000321.3(RB1):c.1104A&gt;T (p.Val368=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1134810|NM_000321.3(RB1):c.1128-9C&gt;T|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1134817|NM_000321.3(RB1):c.246A&gt;G (p.Ser82=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1137269|NM_000321.3(RB1):c.6G&gt;A (p.Pro2=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1138332|NM_000321.3(RB1):c.634C&gt;T (p.Leu212=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1138374|NM_000321.3(RB1):c.2175A&gt;G (p.Val725=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1138883|NM_000321.3(RB1):c.1908C&gt;T (p.Phe636=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1138966|NM_000321.3(RB1):c.2382T&gt;C (p.Ser794=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1139193|NM_000321.3(RB1):c.2326-10T&gt;G|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1139450|NM_000321.3(RB1):c.2211+7A&gt;G|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1139883|NM_000321.3(RB1):c.1814+7A&gt;T|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1139935|NM_000321.3(RB1):c.2061C&gt;T (p.Thr687=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1141974|NM_000321.3(RB1):c.813A&gt;G (p.Thr271=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1143614|NM_000321.3(RB1):c.1146C&gt;A (p.Ile382=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1143679|NM_000321.3(RB1):c.1216-8T&gt;C|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1145417|NM_000321.3(RB1):c.2772C&gt;T (p.Asn924=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1145921|NM_000321.3(RB1):c.1851T&gt;C (p.Gly617=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1146615|NM_000321.3(RB1):c.294G&gt;A (p.Leu98=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1147013|NM_000321.3(RB1):c.1881T&gt;C (p.Asn627=)|single nucleotide variant|Likely benign|RB1|criteria provided, single submitter|13","1147966|NM_000321.3(RB1):c.1584T&gt;C (p.Phe528=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13","1148538|NM_000321.3(RB1):c.99A&gt;G (p.Pro33=)|single nucleotide variant|Likely benign|RB1|criteria provided, multiple submitters, no conflicts|13"]}]}