ClinVar Miner

List of variants in gene RB1 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 101
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HGVS dbSNP gnomAD frequency
NM_000321.3(RB1):c.2106+135_2106+137del rs1566235895 0.06275
NM_000321.3(RB1):c.2106+83T>C rs183550522 0.03467
NM_000321.3(RB1):c.2106+67T>C rs538405205 0.03299
NM_000321.3(RB1):c.1216-29A>G rs3092886 0.02593
NM_000321.3(RB1):c.2106+116del rs1566235804 0.02107
NM_000321.3(RB1):c.2106+118T>C rs543633222 0.02056
NM_000321.3(RB1):c.2713+166A>T rs77520761 0.01543
NM_000321.3(RB1):c.380+193G>T rs77400127 0.01381
NM_000321.3(RB1):c.264+182T>C rs146247663 0.01319
NM_000321.3(RB1):c.861+247dup rs558755474 0.01319
NM_000321.3(RB1):c.1498+73G>A rs112189207 0.01287
NM_000321.3(RB1):c.264+186T>A rs189562489 0.01277
NM_000321.3(RB1):c.264+187G>A rs181781596 0.01263
NM_000321.3(RB1):c.2490-1323C>T rs55926808 0.01180
NM_000321.3(RB1):c.718+138G>A rs3092869 0.01160
NM_000321.3(RB1):c.264+198T>C rs1342739317 0.01119
NM_000321.3(RB1):c.500+251T>C rs4151458 0.01102
NM_000321.3(RB1):c.719-178T>C rs3092885 0.01102
NM_000321.3(RB1):c.264+200C>G rs1219836019 0.01088
NM_000321.3(RB1):c.137+94C>T rs191994935 0.01058
NM_000321.3(RB1):c.501-38G>A rs3092884 0.01032
NM_000321.3(RB1):c.718+35A>T rs3092868 0.01015
NM_000321.3(RB1):c.500+336G>A rs4151461 0.00925
NM_000321.3(RB1):c.500+171A>G rs4151456 0.00923
NM_000321.3(RB1):c.608-3208A>G rs56871512 0.00923
NM_000321.3(RB1):c.1961-156T>C rs4151595 0.00919
NM_000321.3(RB1):c.940-111C>T rs4151501 0.00913
NM_000321.3(RB1):c.*184A>T rs4151630 0.00902
NM_000321.3(RB1):c.2106+53_2106+55del rs562259461 0.00896
NM_000321.3(RB1):c.2212-145T>C rs114464494 0.00896
NM_000321.3(RB1):c.1498+65T>G rs78704248 0.00718
NM_000321.3(RB1):c.939+87T>C rs3092863 0.00717
NM_000321.3(RB1):c.500+46A>G rs3092901 0.00606
NM_000321.3(RB1):c.2521-11G>A rs4151624 0.00570
NM_000321.3(RB1):c.1696-154G>A rs77145577 0.00569
NM_000321.3(RB1):c.500+199A>T rs4151457 0.00569
NM_000321.3(RB1):c.2664-182A>G rs2000992 0.00559
NM_000321.3(RB1):c.2490-1169G>A rs75052176 0.00406
NM_000321.3(RB1):c.2490-1329C>T rs150635376 0.00400
NM_000321.3(RB1):c.607+146A>G rs180962798 0.00371
NM_000321.3(RB1):c.1695+273T>G rs540672435 0.00369
NM_000321.3(RB1):c.1390-11A>G rs200658795 0.00365
NM_000321.3(RB1):c.1332+327A>G rs189969991 0.00334
NM_000321.3(RB1):c.1632A>G (p.Arg544=) rs143948310 0.00245
NM_000321.3(RB1):c.42C>T (p.Ala14=) rs148980395 0.00162
NM_000321.3(RB1):c.380+10C>G rs187110786 0.00158
NM_000321.3(RB1):c.1961-12T>C rs201697122 0.00104
NM_000321.3(RB1):c.1129A>T (p.Thr377Ser) rs146897002 0.00080
NM_000321.3(RB1):c.920C>T (p.Thr307Ile) rs183898408 0.00079
NM_000321.3(RB1):c.2566G>A (p.Asp856Asn) rs149359120 0.00075
NM_000321.3(RB1):c.1770T>C (p.Cys590=) rs145310579 0.00062
NM_000321.3(RB1):c.1966C>T (p.Arg656Trp) rs142509759 0.00059
NM_000321.3(RB1):c.1707A>G (p.Leu569=) rs3092895 0.00052
NM_000321.3(RB1):c.411A>T (p.Glu137Asp) rs3092902 0.00040
NM_000321.3(RB1):c.929G>A (p.Gly310Glu) rs200844292 0.00029
NM_000321.3(RB1):c.1491A>T (p.Thr497=) rs150115447 0.00015
NM_000321.3(RB1):c.1306C>A (p.Gln436Lys) rs4151534 0.00014
NM_000321.3(RB1):c.2463A>G (p.Thr821=) rs370088029 0.00011
NM_000321.3(RB1):c.1862G>A (p.Arg621His) rs373601944 0.00009
NM_000321.3(RB1):c.2003G>A (p.Arg668His) rs551747882 0.00005
NM_000321.3(RB1):c.1619G>T (p.Gly540Val) rs769696726 0.00004
NM_000321.3(RB1):c.1814+11T>C rs771369373 0.00004
NM_000321.3(RB1):c.462G>A (p.Lys154=) rs369830657 0.00004
NM_000321.3(RB1):c.1696-14C>T rs776912915 0.00002
NM_000321.3(RB1):c.124C>T (p.Leu42=) rs1312883856 0.00001
NM_000321.3(RB1):c.2277C>T (p.Val759=) rs1949430859 0.00001
NM_000321.3(RB1):c.2436A>G (p.Pro812=) rs1276641790 0.00001
NM_000321.3(RB1):c.2714-10C>T rs1060504825 0.00001
NM_000321.3(RB1):c.539C>T (p.Ser180Leu) rs367654488 0.00001
NM_000321.3(RB1):c.1131T>C (p.Thr377=) rs1414284893
NM_000321.3(RB1):c.1218C>T (p.Asn406=) rs1593453983
NM_000321.3(RB1):c.1390-71_1390-70del rs35427721
NM_000321.3(RB1):c.1421+27T>A
NM_000321.3(RB1):c.1470T>A (p.Ala490=)
NM_000321.3(RB1):c.1499-10del rs148580581
NM_000321.3(RB1):c.15C>A (p.Thr5=) rs1593411934
NM_000321.3(RB1):c.1695+268del rs200594775
NM_000321.3(RB1):c.1695+74dup rs548436965
NM_000321.3(RB1):c.1861C>A (p.Arg621Ser) rs367578442
NM_000321.3(RB1):c.2062C>T (p.Leu688=)
NM_000321.3(RB1):c.207T>C (p.His69=) rs759594127
NM_000321.3(RB1):c.2106+104_2106+106del rs1566235767
NM_000321.3(RB1):c.2106+108_2106+110del rs1482716468
NM_000321.3(RB1):c.2106+146_2106+147del rs375084275
NM_000321.3(RB1):c.2106+96_2106+98del rs1566235741
NM_000321.3(RB1):c.2212-15_2212-12del rs752717404
NM_000321.3(RB1):c.2232C>A (p.Ile744=)
NM_000321.3(RB1):c.2310G>A (p.Gln770=) rs777040395
NM_000321.3(RB1):c.2406G>A (p.Gly802=) rs866638680
NM_000321.3(RB1):c.2455C>T (p.Leu819=) rs375751988
NM_000321.3(RB1):c.2460A>G (p.Pro820=) rs1555294628
NM_000321.3(RB1):c.2489+249G>T rs4151603
NM_000321.3(RB1):c.265-9576C>T
NM_000321.3(RB1):c.45_53del (p.Ala16_Ala18del) rs572454921
NM_000321.3(RB1):c.540-23dup
NM_000321.3(RB1):c.540-265dup rs58957756
NM_000321.3(RB1):c.570G>A (p.Val190=) rs775061547
NM_000321.3(RB1):c.608-144del rs547128110
NM_000321.3(RB1):c.608-4del rs762805947
NM_000321.3(RB1):c.72G>C (p.Pro24=) rs1333596916
NM_000321.3(RB1):c.940-21C>A rs559042622

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