ClinVar Miner

List of variants in gene RB1 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP
NM_000321.2(RB1):c.1128-5del rs886038280
NM_000321.2(RB1):c.114C>T (p.Gly38=) rs1369823342
NM_000321.2(RB1):c.1216-10C>T rs1060504823
NM_000321.2(RB1):c.1216-6C>T rs1453083586
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.1390-9C>G rs150700378
NM_000321.2(RB1):c.1463C>T (p.Ala488Val) rs780248969
NM_000321.2(RB1):c.1467C>T (p.Cys489=) rs141608408
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.1704T>G (p.Pro568=) rs1555293625
NM_000321.2(RB1):c.180A>G (p.Leu60=) rs878853948
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.1961-6C>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.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.2106+8A>G rs750581965
NM_000321.2(RB1):c.2145G>A (p.Lys715=) rs1555294515
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.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.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.2521-4G>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.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.399C>T (p.Asn133=) rs765277265
NM_000321.2(RB1):c.417T>C (p.Asp139=) rs1555283135
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.608-9T>G rs781780669
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.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.862-4del rs1555285114
NM_000321.2(RB1):c.862-8T>C rs745767704

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