ClinVar Miner

List of variants in gene RBM20 reported as benign for not provided

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Gene type:
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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_001134363.3(RBM20):c.2551-167C>T rs11195343 0.99964
NM_001134363.3(RBM20):c.3573+194A>G rs7895891 0.97073
NM_001134363.3(RBM20):c.1337+32G>A rs6585012 0.75089
NM_001134363.3(RBM20):c.2550+225G>A rs1417634 0.55176
NM_001134363.3(RBM20):c.1338-36A>C rs7898438 0.54481
NM_001134363.3(RBM20):c.2656-153C>T rs10787283 0.53083
NM_001134363.3(RBM20):c.3451+234A>G rs4918595 0.49122
NM_001134363.3(RBM20):c.2550+168T>C rs1832745 0.44671
NM_001134363.3(RBM20):c.3452-237G>A rs4918601 0.43193
NM_001134363.3(RBM20):c.1276-259A>G rs12254016 0.42322
NM_001134363.3(RBM20):c.1800+336C>A rs7090878 0.42174
NM_001134363.3(RBM20):c.1668+264A>G rs12359298 0.39857
NM_001134363.3(RBM20):c.1669-256C>T rs7086491 0.38805
NM_001134363.3(RBM20):c.1880+23T>C rs11195338 0.31080
NM_001134363.3(RBM20):c.1429+154C>T rs7073950 0.21599
NM_001134363.3(RBM20):c.1275+34T>C rs61862866 0.21567
NM_001134363.3(RBM20):c.1275+36G>A rs61862867 0.21544
NM_001134363.3(RBM20):c.1669-131G>A rs7086886 0.18979
NM_001134363.3(RBM20):c.1668+108C>T rs6585014 0.15973
NM_001134363.3(RBM20):c.1337+160G>A rs1570426 0.10850
NC_000010.11:g.110644335C>T rs12783859 0.05599
NM_001134363.3(RBM20):c.1881-214del rs140844165 0.04279
NM_001134363.3(RBM20):c.3316+243C>G rs61862920 0.03948
NM_001134363.3(RBM20):c.1528-205A>G rs74788397 0.03433
NM_001134363.3(RBM20):c.3452-41G>C rs74407586 0.03343
NM_001134363.3(RBM20):c.1338-237A>G rs55873340 0.03185
NM_001134363.3(RBM20):c.1338-234G>A rs7898501 0.02470
NM_001134363.3(RBM20):c.192-31G>A rs114622030 0.01739
NM_001134363.3(RBM20):c.191+106C>T rs114033006 0.01522
NM_001134363.3(RBM20):c.1364C>T (p.Ser455Leu) rs189569984 0.00554
NM_001134363.3(RBM20):c.2318A>G (p.Lys773Arg) rs181769913 0.00324
NM_001134363.3(RBM20):c.*3289C>T rs144896119 0.00310
NM_001134363.3(RBM20):c.*999A>G rs138114979 0.00234
NM_001134363.3(RBM20):c.1179C>T (p.Pro393=) rs200588338 0.00078
NM_001134363.3(RBM20):c.680G>T (p.Gly227Val) rs202238753 0.00066
NM_001134363.3(RBM20):c.*1360G>A rs572337036 0.00048
NM_001134363.3(RBM20):c.2244T>G (p.Ser748=) rs727503388 0.00007
NM_001134363.3(RBM20):c.2232C>T (p.Asn744=) rs975320203 0.00003
NM_001134363.3(RBM20):c.1527+36_1527+41del rs200035751
NM_001134363.3(RBM20):c.1528-211AT[8] rs368264922
NM_001134363.3(RBM20):c.1880+4_1880+6dup rs397516597
NM_001134363.3(RBM20):c.192-164del rs34363441
NM_001134363.3(RBM20):c.192-165_192-164del rs34363441
NM_001134363.3(RBM20):c.3317-28_3317-22del rs201149204
NM_001134363.3(RBM20):c.3317-30_3317-22del rs201149204
NM_001134363.3(RBM20):c.3317-34_3317-22del rs201149204
NM_001134363.3(RBM20):c.3317-35_3317-22del rs201149204
NM_001134363.3(RBM20):c.3451+277del rs72199900
NM_001134363.3(RBM20):c.3451+293dup rs1338701346

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