ClinVar Miner

List of variants in gene TP53 reported as uncertain significance by All of Us Research Program, National Institutes of Health

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Gene type:
ClinVar version:
Total variants: 146
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.460G>A (p.Gly154Ser) rs137852789 0.00004
NM_000546.6(TP53):c.554G>A (p.Ser185Asn) rs150607408 0.00004
NM_000546.6(TP53):c.868C>T (p.Arg290Cys) rs770374782 0.00004
NM_000546.6(TP53):c.998G>A (p.Arg333His) rs573154688 0.00004
NM_000546.6(TP53):c.105G>C (p.Leu35Phe) rs121912661 0.00003
NM_000546.6(TP53):c.1120G>C (p.Gly374Arg) rs587781858 0.00003
NM_000546.6(TP53):c.188C>G (p.Ala63Gly) rs372201428 0.00003
NM_000546.6(TP53):c.214C>G (p.Pro72Ala) rs587782769 0.00003
NM_000546.6(TP53):c.382C>A (p.Pro128Thr) rs1555526327 0.00003
NM_000546.6(TP53):c.467G>A (p.Arg156His) rs371524413 0.00003
NM_000546.6(TP53):c.509C>T (p.Thr170Met) rs779000871 0.00003
NM_000546.6(TP53):c.464C>G (p.Thr155Ser) rs786202752 0.00002
NM_000546.6(TP53):c.665C>T (p.Pro222Leu) rs146340390 0.00002
NM_000546.6(TP53):c.997C>T (p.Arg333Cys) rs769934890 0.00002
NM_000546.6(TP53):c.1001G>A (p.Gly334Glu) rs1286563734 0.00001
NM_000546.6(TP53):c.1003C>T (p.Arg335Cys) rs375444154 0.00001
NM_000546.6(TP53):c.1004G>A (p.Arg335His) rs771939956 0.00001
NM_000546.6(TP53):c.1025G>A (p.Arg342Gln) rs375338359 0.00001
NM_000546.6(TP53):c.1048C>G (p.Leu350Val) rs768046010 0.00001
NM_000546.6(TP53):c.1060C>A (p.Gln354Lys) rs755394212 0.00001
NM_000546.6(TP53):c.1061A>G (p.Gln354Arg) rs752142489 0.00001
NM_000546.6(TP53):c.1066G>C (p.Gly356Arg) rs766786605 0.00001
NM_000546.6(TP53):c.1078G>A (p.Gly360Arg) rs786203298 0.00001
NM_000546.6(TP53):c.1082G>A (p.Gly361Glu) rs587781663 0.00001
NM_000546.6(TP53):c.1136G>A (p.Arg379His) rs863224682 0.00001
NM_000546.6(TP53):c.1150A>G (p.Met384Val) rs730882009 0.00001
NM_000546.6(TP53):c.1151T>C (p.Met384Thr) rs1060501196 0.00001
NM_000546.6(TP53):c.149T>C (p.Ile50Thr) rs370502517 0.00001
NM_000546.6(TP53):c.14A>G (p.Gln5Arg) rs781595324 0.00001
NM_000546.6(TP53):c.155A>G (p.Gln52Arg) rs774656101 0.00001
NM_000546.6(TP53):c.171C>A (p.Asp57Glu) rs587782776 0.00001
NM_000546.6(TP53):c.188C>T (p.Ala63Val) rs372201428 0.00001
NM_000546.6(TP53):c.21T>A (p.Asp7Glu) rs587781277 0.00001
NM_000546.6(TP53):c.221C>T (p.Ala74Val) rs587781832 0.00001
NM_000546.6(TP53):c.250G>A (p.Ala84Thr) rs587781307 0.00001
NM_000546.6(TP53):c.322G>A (p.Gly108Ser) rs587782461 0.00001
NM_000546.6(TP53):c.328C>T (p.Arg110Cys) rs587781371 0.00001
NM_000546.6(TP53):c.393C>A (p.Asn131Lys) rs769270327 0.00001
NM_000546.6(TP53):c.457C>T (p.Pro153Ser) rs1064795860 0.00001
NM_000546.6(TP53):c.469G>A (p.Val157Ile) rs121912654 0.00001
NM_000546.6(TP53):c.472C>T (p.Arg158Cys) rs587780068 0.00001
NM_000546.6(TP53):c.480G>A (p.Met160Ile) rs772354334 0.00001
NM_000546.6(TP53):c.500A>C (p.Gln167Pro) rs1319163924 0.00001
NM_000546.6(TP53):c.530C>T (p.Pro177Leu) rs751477326 0.00001
NM_000546.6(TP53):c.572C>G (p.Pro191Arg) rs587778718 0.00001
NM_000546.6(TP53):c.587G>A (p.Arg196Gln) rs483352697 0.00001
NM_000546.6(TP53):c.604C>T (p.Arg202Cys) rs587780072 0.00001
NM_000546.6(TP53):c.605G>A (p.Arg202His) rs587778719 0.00001
NM_000546.6(TP53):c.686G>A (p.Cys229Tyr) rs1064793603 0.00001
NM_000546.6(TP53):c.760A>G (p.Ile254Val) rs746601313 0.00001
NM_000546.6(TP53):c.782+6G>A rs1008479744 0.00001
NM_000546.6(TP53):c.800G>A (p.Arg267Gln) rs587780075 0.00001
NM_000546.6(TP53):c.848G>A (p.Arg283His) rs371409680 0.00001
NM_000546.6(TP53):c.850A>T (p.Thr284Ser) rs1204379654 0.00001
NM_000546.6(TP53):c.884C>T (p.Pro295Leu) rs751713111 0.00001
NM_000546.6(TP53):c.907A>G (p.Ser303Gly) rs587782391 0.00001
NM_000546.6(TP53):c.920C>T (p.Ala307Val) rs1457582183 0.00001
NM_000546.6(TP53):c.949C>A (p.Gln317Lys) rs764735889 0.00001
NM_000546.6(TP53):c.953C>T (p.Pro318Leu) rs1555524975 0.00001
NM_000546.6(TP53):c.97-5T>G rs768373702 0.00001
NM_000546.6(TP53):c.970G>C (p.Asp324His) rs1064794810 0.00001
NM_000546.6(TP53):c.974G>T (p.Gly325Val) rs121912659 0.00001
NM_000546.6(TP53):c.100C>A (p.Pro34Thr) rs786201968
NM_000546.6(TP53):c.100C>G (p.Pro34Ala) rs786201968
NM_000546.6(TP53):c.1014C>G (p.Phe338Leu) rs150293825
NM_000546.6(TP53):c.1015G>C (p.Glu339Gln) rs17882252
NM_000546.6(TP53):c.1023C>A (p.Phe341Leu) rs864622369
NM_000546.6(TP53):c.1079G>A (p.Gly360Glu) rs35993958
NM_000546.6(TP53):c.1100+5G>A rs889930337
NM_000546.6(TP53):c.110C>T (p.Ser37Phe) rs1567557177
NM_000546.6(TP53):c.1118A>G (p.Lys373Arg) rs1567540504
NM_000546.6(TP53):c.1120G>T (p.Gly374Cys) rs587781858
NM_000546.6(TP53):c.1135C>A (p.Arg379Ser) rs749061599
NM_000546.6(TP53):c.1135C>T (p.Arg379Cys) rs749061599
NM_000546.6(TP53):c.1152G>A (p.Met384Ile) rs1597345344
NM_000546.6(TP53):c.1160C>G (p.Thr387Arg) rs927888647
NM_000546.6(TP53):c.1163A>C (p.Glu388Ala) rs587781736
NM_000546.6(TP53):c.11C>T (p.Pro4Leu) rs878854064
NM_000546.6(TP53):c.139C>G (p.Pro47Ala) rs1800371
NM_000546.6(TP53):c.144C>A (p.Asp48Glu) rs587781460
NM_000546.6(TP53):c.145G>C (p.Asp49His) rs587780728
NM_000546.6(TP53):c.146A>G (p.Asp49Gly) rs759728549
NM_000546.6(TP53):c.182A>G (p.Asp61Gly) rs1460793472
NM_000546.6(TP53):c.199C>G (p.Pro67Ala) rs2073476832
NM_000546.6(TP53):c.211C>G (p.Pro71Ala) rs1567556576
NM_000546.6(TP53):c.215C>A (p.Pro72His) rs1042522
NM_000546.6(TP53):c.233C>G (p.Ala78Gly) rs876658527
NM_000546.6(TP53):c.275C>T (p.Pro92Leu) rs1210700121
NM_000546.6(TP53):c.277dup (p.Leu93fs)
NM_000546.6(TP53):c.283TCT[1] (p.Ser96del) rs878854068
NM_000546.6(TP53):c.289G>C (p.Val97Leu) rs730882023
NM_000546.6(TP53):c.28G>T (p.Val10Phe) rs535274413
NM_000546.6(TP53):c.303A>T (p.Lys101Asn) rs878854069
NM_000546.6(TP53):c.305C>T (p.Thr102Ile) rs786202717
NM_000546.6(TP53):c.314G>A (p.Gly105Asp) rs587781504
NM_000546.6(TP53):c.344A>G (p.His115Arg) rs730881996
NM_000546.6(TP53):c.35C>T (p.Pro12Leu) rs1482497533
NM_000546.6(TP53):c.368C>T (p.Thr123Ile) rs1555526486
NM_000546.6(TP53):c.37C>G (p.Pro13Ala) rs1060501208
NM_000546.6(TP53):c.380C>A (p.Ser127Tyr) rs730881999
NM_000546.6(TP53):c.46C>A (p.Gln16Lys) rs2151047550
NM_000546.6(TP53):c.493C>A (p.Gln165Lys) rs730882001
NM_000546.6(TP53):c.507G>T (p.Met169Ile) rs2073372247
NM_000546.6(TP53):c.516T>G (p.Val172=) rs749309577
NM_000546.6(TP53):c.522G>C (p.Arg174Ser) rs2151030685
NM_000546.6(TP53):c.535_537del (p.His179del) rs2543594576
NM_000546.6(TP53):c.542G>T (p.Arg181Leu) rs397514495
NM_000546.6(TP53):c.559+4A>G rs1357840734
NM_000546.6(TP53):c.576G>T (p.Gln192His) rs2073344721
NM_000546.6(TP53):c.589G>A (p.Val197Met) rs786204041
NM_000546.6(TP53):c.596G>A (p.Gly199Glu) rs1555525857
NM_000546.6(TP53):c.625A>G (p.Arg209Gly) rs1429743956
NM_000546.6(TP53):c.644G>C (p.Ser215Thr) rs587782177
NM_000546.6(TP53):c.645T>A (p.Ser215Arg) rs1057520001
NM_000546.6(TP53):c.676G>A (p.Gly226Ser) rs1597365543
NM_000546.6(TP53):c.686G>C (p.Cys229Ser) rs1064793603
NM_000546.6(TP53):c.688A>G (p.Thr230Ala) rs1597365431
NM_000546.6(TP53):c.692C>T (p.Thr231Ile) rs1555525564
NM_000546.6(TP53):c.721T>G (p.Ser241Ala) rs1057520002
NM_000546.6(TP53):c.727A>G (p.Met243Val) rs786203117
NM_000546.6(TP53):c.752T>A (p.Ile251Asn) rs730882027
NM_000546.6(TP53):c.754_765del (p.Leu252_Ile255del) rs2543558116
NM_000546.6(TP53):c.782+3C>T rs1555525425
NM_000546.6(TP53):c.785G>T (p.Gly262Val) rs1131691025
NM_000546.6(TP53):c.7G>A (p.Glu3Lys) rs2073524362
NM_000546.6(TP53):c.830G>A (p.Cys277Tyr) rs763098116
NM_000546.6(TP53):c.830G>T (p.Cys277Phe) rs763098116
NM_000546.6(TP53):c.845G>A (p.Arg282Gln) rs730882008
NM_000546.6(TP53):c.850A>G (p.Thr284Ala) rs1204379654
NM_000546.6(TP53):c.865C>T (p.Leu289Phe) rs1555525154
NM_000546.6(TP53):c.870C>T (p.Arg290=) rs1555525135
NM_000546.6(TP53):c.871A>G (p.Lys291Glu) rs1555525126
NM_000546.6(TP53):c.877G>A (p.Gly293Arg) rs587780076
NM_000546.6(TP53):c.892G>A (p.Glu298Lys) rs201744589
NM_000546.6(TP53):c.917G>A (p.Arg306Gln) rs1048095040
NM_000546.6(TP53):c.919+3A>G rs876659784
NM_000546.6(TP53):c.919G>A (p.Ala307Thr) rs2151013719
NM_000546.6(TP53):c.920-6T>G rs2151012543
NM_000546.6(TP53):c.925C>T (p.Pro309Ser) rs1555525012
NM_000546.6(TP53):c.930C>A (p.Asn310Lys) rs876660829
NM_000546.6(TP53):c.946C>T (p.Pro316Ser) rs772773208
NM_000546.6(TP53):c.959A>C (p.Lys320Thr) rs2151011608
NM_000546.6(TP53):c.97-3C>T rs786203749
NM_000546.6(TP53):c.974G>A (p.Gly325Glu) rs121912659
NM_000546.6(TP53):c.986C>T (p.Thr329Ile) rs969930693
NM_000546.6(TP53):c.994-5T>G rs375273756

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