ClinVar Miner

List of variants in gene RB1 reported as likely benign

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Gene type:
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Total variants: 123
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HGVS dbSNP
NM_000321.2(RB1):c.*1268G>A rs571383547
NM_000321.2(RB1):c.*1527_*1528del rs540108904
NM_000321.2(RB1):c.*1687T>C rs4151635
NM_000321.2(RB1):c.*172G>A rs143536240
NM_000321.2(RB1):c.*184A>T rs4151630
NM_000321.2(RB1):c.*463T>A rs4151631
NM_000321.2(RB1):c.*703G>T rs139023385
NM_000321.2(RB1):c.*964C>G rs4151633
NM_000321.2(RB1):c.1128-5del rs886038280
NM_000321.2(RB1):c.1129A>T (p.Thr377Ser) rs146897002
NM_000321.2(RB1):c.1131T>C (p.Thr377=) rs1414284893
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.1216-10C>T rs1060504823
NM_000321.2(RB1):c.1216-29A>G rs3092886
NM_000321.2(RB1):c.1216-6C>T rs1453083586
NM_000321.2(RB1):c.1218C>T (p.Asn406=)
NM_000321.2(RB1):c.1306C>A (p.Gln436Lys) rs4151534
NM_000321.2(RB1):c.1318G>A (p.Glu440Lys) rs1060503078
NM_000321.2(RB1):c.1333-9dup rs766968771
NM_000321.2(RB1):c.1365A>G (p.Arg455=) rs1316896547
NM_000321.2(RB1):c.138-4G>A rs1010049143
NM_000321.2(RB1):c.138-8T>C rs201562657
NM_000321.2(RB1):c.1390-11A>G rs200658795
NM_000321.2(RB1):c.1390-14A>T rs9535023
NM_000321.2(RB1):c.1390-16A>T rs781419356
NM_000321.2(RB1):c.1390-9C>G rs150700378
NM_000321.2(RB1):c.1410T>C (p.Ile470=) rs578226820
NM_000321.2(RB1):c.1463C>T (p.Ala488Val) rs780248969
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.1499-7T>C rs1351161278
NM_000321.2(RB1):c.1499-8A>T rs1555286676
NM_000321.2(RB1):c.1499-9C>T rs201020747
NM_000321.2(RB1):c.1574C>G (p.Ala525Gly) rs4151539
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.1696-4A>G rs143685082
NM_000321.2(RB1):c.1704T>G (p.Pro568=) rs1555293625
NM_000321.2(RB1):c.1707A>G (p.Leu569=) rs3092895
NM_000321.2(RB1):c.1764T>A (p.Ser588=) rs542783532
NM_000321.2(RB1):c.1770T>C (p.Cys590=) rs145310579
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.1814+11T>C
NM_000321.2(RB1):c.1830A>G (p.Val610=) rs1038764979
NM_000321.2(RB1):c.1862G>A (p.Arg621His) rs373601944
NM_000321.2(RB1):c.1961-12T>C rs201697122
NM_000321.2(RB1):c.1961-6C>T rs200501806
NM_000321.2(RB1):c.1989T>C (p.Asn663=) rs780654106
NM_000321.2(RB1):c.1992A>G (p.Thr664=) rs755417160
NM_000321.2(RB1):c.2003G>A (p.Arg668His) rs551747882
NM_000321.2(RB1):c.2016G>A (p.Glu672=) rs1555294098
NM_000321.2(RB1):c.2046C>G (p.Thr682=) rs994129583
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.2091C>G (p.Asp697Glu) rs3092903
NM_000321.2(RB1):c.2106+8A>G rs750581965
NM_000321.2(RB1):c.2145G>A (p.Lys715=) rs1555294515
NM_000321.2(RB1):c.2212-16T>A rs201258424
NM_000321.2(RB1):c.2212-6C>T rs776162179
NM_000321.2(RB1):c.2212-9C>T rs765386327
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.2325+10A>G rs763525092
NM_000321.2(RB1):c.2356C>T (p.Pro786Ser) rs754507551
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.2460A>T (p.Pro820=) rs1555294628
NM_000321.2(RB1):c.2463A>G (p.Thr821=) rs370088029
NM_000321.2(RB1):c.2489+7G>A rs752607904
NM_000321.2(RB1):c.2517C>T (p.Phe839=) rs759188465
NM_000321.2(RB1):c.2521-11G>A rs4151624
NM_000321.2(RB1):c.2521-4G>T rs902298592
NM_000321.2(RB1):c.2521-7T>A rs371150038
NM_000321.2(RB1):c.2521-9A>C rs949077145
NM_000321.2(RB1):c.2559T>C (p.Cys853=) rs148327780
NM_000321.2(RB1):c.2634T>C (p.Asp878=) rs750293921
NM_000321.2(RB1):c.264+20G>A rs200985890
NM_000321.2(RB1):c.2643A>C (p.Gly881=) rs1060504826
NM_000321.2(RB1):c.2663+8C>A rs747518543
NM_000321.2(RB1):c.2663+8C>G rs747518543
NM_000321.2(RB1):c.2664-9A>C rs369154092
NM_000321.2(RB1):c.2714-10C>T rs1060504825
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.2757C>T (p.Ser919=) rs1060504824
NM_000321.2(RB1):c.285A>G (p.Lys95=) rs755688480
NM_000321.2(RB1):c.30C>G (p.Ala10=) rs530961288
NM_000321.2(RB1):c.30C>T (p.Ala10=) rs530961288
NM_000321.2(RB1):c.342G>A (p.Ser114=) rs748093967
NM_000321.2(RB1):c.380+10C>G rs187110786
NM_000321.2(RB1):c.380+12T>C rs3092881
NM_000321.2(RB1):c.399C>T (p.Asn133=) rs765277265
NM_000321.2(RB1):c.417T>C (p.Asp139=) rs1555283135
NM_000321.2(RB1):c.42C>T (p.Ala14=) rs148980395
NM_000321.2(RB1):c.540-9G>C rs1340503453
NM_000321.2(RB1):c.570G>A (p.Val190=) rs775061547
NM_000321.2(RB1):c.59C>T (p.Pro20Leu) rs587778637
NM_000321.2(RB1):c.607+8C>T rs1555283680
NM_000321.2(RB1):c.608-10T>C rs1039235140
NM_000321.2(RB1):c.608-4del rs762805947
NM_000321.2(RB1):c.608-9T>G rs781780669
NM_000321.2(RB1):c.628G>T (p.Asp210Tyr) rs148992508
NM_000321.2(RB1):c.658C>T (p.Leu220=) rs367960214
NM_000321.2(RB1):c.66A>C (p.Ala22=) rs1014225642
NM_000321.2(RB1):c.66A>G (p.Ala22=) rs1014225642
NM_000321.2(RB1):c.69G>A (p.Pro23=) rs746662122
NM_000321.2(RB1):c.69_71GCC[3] (p.Pro29del) rs587778823
NM_000321.2(RB1):c.719-8T>C rs754589578
NM_000321.2(RB1):c.720A>G (p.Lys240=) rs1555284919
NM_000321.2(RB1):c.783A>G (p.Ala261=) rs759311626
NM_000321.2(RB1):c.810T>C (p.Asp270=) rs1555284937
NM_000321.2(RB1):c.81C>G (p.Pro27=) rs1555279227
NM_000321.2(RB1):c.862-15C>A rs115108608
NM_000321.2(RB1):c.862-4del rs1555285114
NM_000321.2(RB1):c.862-8T>C rs745767704
NM_000321.2(RB1):c.920C>T (p.Thr307Ile) rs183898408
NM_000321.2(RB1):c.929G>A (p.Gly310Glu) rs200844292

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