ClinVar Miner

List of variants in gene RB1 reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 92
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HGVS dbSNP
NM_000321.2(RB1):c.111C>T (p.Ser37=) rs1411090163
NM_000321.2(RB1):c.1129A>T (p.Thr377Ser) rs146897002
NM_000321.2(RB1):c.113G>A (p.Gly38Asp) rs766529534
NM_000321.2(RB1):c.1140C>T (p.Asn380=) rs117865557
NM_000321.2(RB1):c.114C>T (p.Gly38=) rs1369823342
NM_000321.2(RB1):c.1215C>T (p.Asn405=) rs758187955
NM_000321.2(RB1):c.1224A>G (p.Thr408=) rs371805499
NM_000321.2(RB1):c.129T>A (p.Pro43=) rs1304775415
NM_000321.2(RB1):c.1318G>A (p.Glu440Lys) rs1060503078
NM_000321.2(RB1):c.1410T>C (p.Ile470=) rs578226820
NM_000321.2(RB1):c.144G>A (p.Glu48=) rs1021965284
NM_000321.2(RB1):c.1464G>A (p.Ala488=) rs753520981
NM_000321.2(RB1):c.1467C>T (p.Cys489=) rs141608408
NM_000321.2(RB1):c.1491A>T (p.Thr497=) rs150115447
NM_000321.2(RB1):c.1596C>T (p.Ile532=) rs770728170
NM_000321.2(RB1):c.1632A>G (p.Arg544=) rs143948310
NM_000321.2(RB1):c.165T>A (p.Pro55=) rs775560197
NM_000321.2(RB1):c.1707A>G (p.Leu569=) rs3092895
NM_000321.2(RB1):c.1770T>C (p.Cys590=) rs145310579
NM_000321.2(RB1):c.1785T>C (p.Pro595=) rs1194487890
NM_000321.2(RB1):c.1800C>T (p.His600=) rs1555293650
NM_000321.2(RB1):c.180A>G (p.Leu60=) rs878853948
NM_000321.2(RB1):c.1860G>A (p.Thr620=) rs750356534
NM_000321.2(RB1):c.18C>T (p.Pro6=) rs1017683562
NM_000321.2(RB1):c.1914C>A (p.Thr638=) rs770072166
NM_000321.2(RB1):c.1966C>T (p.Arg656Trp) rs142509759
NM_000321.2(RB1):c.1992A>G (p.Thr664=) rs755417160
NM_000321.2(RB1):c.1992A>T (p.Thr664=) rs755417160
NM_000321.2(RB1):c.2040C>A (p.Ile680=) rs1593534695
NM_000321.2(RB1):c.2049T>C (p.Leu683=) rs1048847950
NM_000321.2(RB1):c.2076T>C (p.Tyr692=) rs1060504827
NM_000321.2(RB1):c.207T>C (p.His69=) rs759594127
NM_000321.2(RB1):c.2145G>A (p.Lys715=) rs1555294515
NM_000321.2(RB1):c.2238A>G (p.Glu746=) rs991505835
NM_000321.2(RB1):c.2244G>A (p.Glu748=) rs1131690911
NM_000321.2(RB1):c.2274G>A (p.Ser758=) rs558114005
NM_000321.2(RB1):c.2406G>A (p.Gly802=) rs866638680
NM_000321.2(RB1):c.2436A>G (p.Pro812=) rs1276641790
NM_000321.2(RB1):c.2455C>G (p.Leu819Val) rs375751988
NM_000321.2(RB1):c.2455C>T (p.Leu819=) rs375751988
NM_000321.2(RB1):c.2463A>G (p.Thr821=) rs370088029
NM_000321.2(RB1):c.2517C>T (p.Phe839=) rs759188465
NM_000321.2(RB1):c.2559T>C (p.Cys853=) rs148327780
NM_000321.2(RB1):c.2570G>A (p.Arg857His) rs144668210
NM_000321.2(RB1):c.2634T>C (p.Asp878=) rs750293921
NM_000321.2(RB1):c.273T>C (p.Tyr91=) rs750136284
NM_000321.2(RB1):c.2754T>C (p.Asp918=) rs878853951
NM_000321.2(RB1):c.30C>G (p.Ala10=) rs530961288
NM_000321.2(RB1):c.342G>A (p.Ser114=) rs748093967
NM_000321.2(RB1):c.367A>G (p.Asn123Asp) rs149800437
NM_000321.2(RB1):c.411A>T (p.Glu137Asp) rs3092902
NM_000321.2(RB1):c.42C>T (p.Ala14=) rs148980395
NM_000321.2(RB1):c.462G>A (p.Lys154=) rs369830657
NM_000321.2(RB1):c.571C>T (p.Leu191=) rs538578527
NM_000321.2(RB1):c.658C>T (p.Leu220=) rs367960214
NM_000321.2(RB1):c.69G>A (p.Pro23=) rs746662122
NM_000321.2(RB1):c.810T>C (p.Asp270=) rs1555284937
NM_000321.2(RB1):c.963C>T (p.Tyr321=) rs377235036
NM_000321.3(RB1):c.1086T>G (p.Leu362=) rs1212481028
NM_000321.3(RB1):c.1389A>G (p.Ser463=) rs1486168292
NM_000321.3(RB1):c.1596C>A (p.Ile532=) rs770728170
NM_000321.3(RB1):c.15C>A (p.Thr5=) rs1593411934
NM_000321.3(RB1):c.1692C>T (p.Leu564=) rs1593457168
NM_000321.3(RB1):c.1749T>G (p.Thr583=) rs913654931
NM_000321.3(RB1):c.1755C>T (p.His585=) rs750305249
NM_000321.3(RB1):c.1827T>C (p.Pro609=) rs1593531889
NM_000321.3(RB1):c.1893A>G (p.Gln631=) rs746361171
NM_000321.3(RB1):c.2127T>C (p.Tyr709=) rs1484231598
NM_000321.3(RB1):c.2349T>A (p.Pro783=) rs753349760
NM_000321.3(RB1):c.2360G>A (p.Arg787Gln) rs748094394
NM_000321.3(RB1):c.2370C>T (p.Tyr790=) rs794727372
NM_000321.3(RB1):c.2432G>A (p.Ser811Asn) rs1220980701
NM_000321.3(RB1):c.2566G>A (p.Asp856Asn) rs149359120
NM_000321.3(RB1):c.2586T>C (p.Ser862=) rs1593547157
NM_000321.3(RB1):c.2607T>G (p.Pro869=) rs762588468
NM_000321.3(RB1):c.2628C>T (p.Arg876=) rs1593547215
NM_000321.3(RB1):c.2679A>G (p.Gly893=) rs751718011
NM_000321.3(RB1):c.270T>C (p.Gly90=) rs1593434172
NM_000321.3(RB1):c.2730A>G (p.Arg910=) rs1245341503
NM_000321.3(RB1):c.2775G>A (p.Lys925=) rs936709957
NM_000321.3(RB1):c.309C>A (p.Ile103=) rs1593434233
NM_000321.3(RB1):c.354T>A (p.Thr118=) rs951251256
NM_000321.3(RB1):c.36C>T (p.Thr12=) rs779180897
NM_000321.3(RB1):c.485T>A (p.Phe162Tyr) rs764881599
NM_000321.3(RB1):c.51C>G (p.Ala17=) rs1593412073
NM_000321.3(RB1):c.540-3T>C rs149703672
NM_000321.3(RB1):c.563C>T (p.Ala188Val) rs1593437973
NM_000321.3(RB1):c.59C>T (p.Pro20Leu) rs587778637
NM_000321.3(RB1):c.744T>C (p.Gly248=) rs1297277579
NM_000321.3(RB1):c.920C>T (p.Thr307Ile) rs183898408
NM_000321.3(RB1):c.929G>A (p.Gly310Glu) rs200844292
NM_000321.3(RB1):c.999A>C (p.Ala333=) rs1254874409

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