ClinVar Miner

Variants in gene TP53 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 205
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.*1175A>C rs78378222 0.00849
NM_000546.6(TP53):c.173C>G (p.Pro58Arg) rs144386518 0.00030
NM_000546.5(TP53):c.319T>C (p.Tyr107His) rs368771578 0.00028
NM_000546.6(TP53):c.704A>G (p.Asn235Ser) rs144340710 0.00025
NM_000546.6(TP53):c.1079G>C (p.Gly360Ala) rs35993958 0.00019
NM_000546.6(TP53):c.935C>G (p.Thr312Ser) rs145151284 0.00018
NM_000546.6(TP53):c.869G>A (p.Arg290His) rs55819519 0.00014
NM_000546.6(TP53):c.97-9C>T rs202217267 0.00011
NM_000546.6(TP53):c.673-37C>T rs374907737 0.00010
NM_000546.6(TP53):c.847C>T (p.Arg283Cys) rs149633775 0.00009
NM_000546.6(TP53):c.993+13G>C rs369599972 0.00009
NM_000546.6(TP53):c.1015G>A (p.Glu339Lys) rs17882252 0.00006
NM_000546.6(TP53):c.248C>T (p.Ala83Val) rs201717599 0.00006
NM_000546.6(TP53):c.920-17C>A rs911934766 0.00006
NM_000546.6(TP53):c.*6T>A rs369567704 0.00005
NM_000546.6(TP53):c.782+12C>T rs17881780 0.00005
NM_000546.6(TP53):c.1096T>G (p.Ser366Ala) rs17881470 0.00004
NM_000546.6(TP53):c.28G>A (p.Val10Ile) rs535274413 0.00004
NM_000546.6(TP53):c.469G>A (p.Val157Ile) rs121912654 0.00004
NM_000546.6(TP53):c.554G>A (p.Ser185Asn) rs150607408 0.00004
NM_000546.6(TP53):c.642T>G (p.His214Gln) rs587781386 0.00004
NM_000546.6(TP53):c.677G>T (p.Gly226Val) rs970212462 0.00004
NM_000546.6(TP53):c.868C>T (p.Arg290Cys) rs770374782 0.00004
NM_000546.6(TP53):c.91G>A (p.Val31Ile) rs201753350 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.329G>A (p.Arg110His) rs11540654 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.-12C>T rs375229869 0.00002
NM_000546.6(TP53):c.1060C>A (p.Gln354Lys) rs755394212 0.00002
NM_000546.6(TP53):c.464C>G (p.Thr155Ser) rs786202752 0.00002
NM_000546.6(TP53):c.466C>T (p.Arg156Cys) rs563378859 0.00002
NM_000546.6(TP53):c.665C>T (p.Pro222Leu) rs146340390 0.00002
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.1066G>C (p.Gly356Arg) rs766786605 0.00001
NM_000546.6(TP53):c.1078G>A (p.Gly360Arg) rs786203298 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.145G>A (p.Asp49Asn) rs587780728 0.00001
NM_000546.6(TP53):c.14A>G (p.Gln5Arg) rs781595324 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.229C>T (p.Pro77Ser) rs753085009 0.00001
NM_000546.6(TP53):c.245C>T (p.Pro82Leu) rs534447939 0.00001
NM_000546.6(TP53):c.250G>A (p.Ala84Thr) rs587781307 0.00001
NM_000546.6(TP53):c.289G>T (p.Val97Phe) rs730882023 0.00001
NM_000546.6(TP53):c.341T>C (p.Leu114Ser) rs781724995 0.00001
NM_000546.6(TP53):c.346T>G (p.Ser116Ala) rs989692988 0.00001
NM_000546.6(TP53):c.353C>T (p.Thr118Ile) rs1064794141 0.00001
NM_000546.6(TP53):c.370T>A (p.Cys124Ser) rs730881997 0.00001
NM_000546.6(TP53):c.376-2dup rs751253294 0.00001
NM_000546.6(TP53):c.399G>A (p.Met133Ile) rs1064795139 0.00001
NM_000546.6(TP53):c.463A>G (p.Thr155Ala) rs772683278 0.00001
NM_000546.6(TP53):c.480G>A (p.Met160Ile) rs772354334 0.00001
NM_000546.6(TP53):c.4G>A (p.Glu2Lys) rs769884991 0.00001
NM_000546.6(TP53):c.556G>A (p.Asp186Asn) rs1060501206 0.00001
NM_000546.6(TP53):c.566C>T (p.Ala189Val) rs121912665 0.00001
NM_000546.6(TP53):c.572C>G (p.Pro191Arg) rs587778718 0.00001
NM_000546.6(TP53):c.604C>T (p.Arg202Cys) rs587780072 0.00001
NM_000546.6(TP53):c.673-3T>C rs1214646363 0.00001
NM_000546.6(TP53):c.74+9A>C rs1057517593 0.00001
NM_000546.6(TP53):c.760A>G (p.Ile254Val) rs746601313 0.00001
NM_000546.6(TP53):c.783-10T>C rs377590379 0.00001
NM_000546.6(TP53):c.850A>T (p.Thr284Ser) rs1204379654 0.00001
NM_000546.6(TP53):c.851C>T (p.Thr284Ile) rs863224685 0.00001
NM_000546.6(TP53):c.861G>C (p.Glu287Asp) rs748891343 0.00001
NM_000546.6(TP53):c.875A>G (p.Lys292Arg) rs121912663 0.00001
NM_000546.6(TP53):c.877G>T (p.Gly293Trp) rs587780076 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.919+7A>C rs199527475 0.00001
NM_000546.6(TP53):c.943T>A (p.Ser315Thr) rs762620193 0.00001
NM_000546.6(TP53):c.949C>A (p.Gln317Lys) rs764735889 0.00001
NM_000546.6(TP53):c.96+15T>C rs200053580 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.101C>G (p.Pro34Arg) rs1322947350
NM_000546.6(TP53):c.103T>A (p.Leu35Met) rs1060501211
NM_000546.6(TP53):c.1054G>T (p.Asp352Tyr) rs1555524394
NM_000546.6(TP53):c.1064C>T (p.Ala355Val) rs1555524382
NM_000546.6(TP53):c.1066G>A (p.Gly356Arg)
NM_000546.6(TP53):c.1072G>A (p.Glu358Lys) rs587782237
NM_000546.6(TP53):c.1073A>T (p.Glu358Val) rs773553186
NM_000546.6(TP53):c.1079G>T (p.Gly360Val) rs35993958
NM_000546.6(TP53):c.107C>A (p.Pro36Gln) rs587781866
NM_000546.6(TP53):c.1093C>T (p.His365Tyr) rs267605075
NM_000546.6(TP53):c.1100+8A>G rs878854062
NM_000546.6(TP53):c.1102C>T (p.His368Tyr) rs786204227
NM_000546.6(TP53):c.1104C>A (p.His368Gln) rs1289241865
NM_000546.6(TP53):c.1104C>G (p.His368Gln) rs1289241865
NM_000546.6(TP53):c.1115A>G (p.Lys372Arg) rs876658876
NM_000546.6(TP53):c.1118A>G (p.Lys373Arg) rs1567540504
NM_000546.6(TP53):c.1130C>T (p.Thr377Ile) rs1597345549
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.1136G>T (p.Arg379Leu) rs863224682
NM_000546.6(TP53):c.1163A>C (p.Glu388Ala) rs587781736
NM_000546.6(TP53):c.116C>T (p.Ala39Val) rs1353016807
NM_000546.6(TP53):c.1177G>A (p.Asp393Asn) rs1192921623
NM_000546.6(TP53):c.1177G>C (p.Asp393His) rs1192921623
NM_000546.6(TP53):c.118A>G (p.Met40Val) rs1597375159
NM_000546.6(TP53):c.11C>G (p.Pro4Arg) rs878854064
NM_000546.6(TP53):c.11C>T (p.Pro4Leu) rs878854064
NM_000546.6(TP53):c.121G>A (p.Asp41Asn) rs1555526789
NM_000546.6(TP53):c.125A>G (p.Asp42Gly) rs587781767
NM_000546.6(TP53):c.132G>A (p.Met44Ile) rs1060501190
NM_000546.6(TP53):c.139C>A (p.Pro47Thr) rs1800371
NM_000546.6(TP53):c.140C>G (p.Pro47Arg) rs1597375038
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.149T>C (p.Ile50Thr) rs370502517
NM_000546.6(TP53):c.183T>A (p.Asp61Glu) rs1597374797
NM_000546.6(TP53):c.198G>A (p.Met66Ile) rs1555526711
NM_000546.6(TP53):c.19G>C (p.Asp7His) rs587782646
NM_000546.6(TP53):c.205G>A (p.Ala69Thr) rs1567556618
NM_000546.6(TP53):c.211C>G (p.Pro71Ala) rs1567556576
NM_000546.6(TP53):c.214C>A (p.Pro72Thr) rs587782769
NM_000546.6(TP53):c.214_215delinsTG (p.Pro72Cys) rs730882014
NM_000546.6(TP53):c.215C>A (p.Pro72His) rs1042522
NM_000546.6(TP53):c.215_217delinsGCA (p.Pro72_Val73delinsArgMet)
NM_000546.6(TP53):c.229C>A (p.Pro77Thr) rs753085009
NM_000546.6(TP53):c.22C>A (p.Pro8Thr) rs1597376589
NM_000546.6(TP53):c.233C>G (p.Ala78Gly) rs876658527
NM_000546.6(TP53):c.244C>G (p.Pro82Ala) rs1555526664
NM_000546.6(TP53):c.248C>A (p.Ala83Glu) rs201717599
NM_000546.6(TP53):c.256G>C (p.Ala86Pro)
NM_000546.6(TP53):c.257C>T (p.Ala86Val) rs1597374264
NM_000546.6(TP53):c.263C>T (p.Ala88Val) rs1555526631
NM_000546.6(TP53):c.266C>T (p.Pro89Leu) rs730881994
NM_000546.6(TP53):c.275C>T (p.Pro92Leu) rs1210700121
NM_000546.6(TP53):c.27C>G (p.Ser9Arg) rs757282628
NM_000546.6(TP53):c.28G>C (p.Val10Leu) rs535274413
NM_000546.6(TP53):c.304A>T (p.Thr102Ser) rs1567555968
NM_000546.6(TP53):c.305C>T (p.Thr102Ile) rs786202717
NM_000546.6(TP53):c.31G>A (p.Glu11Lys) rs201382018
NM_000546.6(TP53):c.31G>C (p.Glu11Gln) rs201382018
NM_000546.6(TP53):c.322G>A (p.Gly108Ser) rs587782461
NM_000546.6(TP53):c.343C>A (p.His115Asn) rs1555526532
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.364G>A (p.Val122Met) rs587781495
NM_000546.6(TP53):c.376-4A>T rs1221388024
NM_000546.6(TP53):c.382C>A (p.Pro128Thr) rs1555526327
NM_000546.6(TP53):c.385G>A (p.Ala129Thr) rs1438095083
NM_000546.6(TP53):c.516T>G (p.Val172=) rs749309577
NM_000546.6(TP53):c.548C>T (p.Ser183Leu) rs1555525970
NM_000546.6(TP53):c.559+8G>A rs775915220
NM_000546.6(TP53):c.604C>G (p.Arg202Gly) rs587780072
NM_000546.6(TP53):c.605G>A (p.Arg202His) rs587778719
NM_000546.6(TP53):c.625A>G (p.Arg209Gly) rs1429743956
NM_000546.6(TP53):c.66A>G (p.Leu22=) rs748527030
NM_000546.6(TP53):c.672+9T>C rs1057521030
NM_000546.6(TP53):c.673-4C>G rs1555525586
NM_000546.6(TP53):c.673-5C>G rs876658684
NM_000546.6(TP53):c.673G>A (p.Val225Ile) rs746504075
NM_000546.6(TP53):c.684C>G (p.Asp228Glu) rs2073267220
NM_000546.6(TP53):c.698A>G (p.His233Arg) rs879254233
NM_000546.6(TP53):c.779C>A (p.Ser260Tyr) rs876658916
NM_000546.6(TP53):c.782+3C>T rs1555525425
NM_000546.6(TP53):c.783-16_783-15del rs1064793810
NM_000546.6(TP53):c.783-4G>A rs1060504160
NM_000546.6(TP53):c.787A>G (p.Asn263Asp) rs72661119
NM_000546.6(TP53):c.79C>A (p.Pro27Thr) rs922736614
NM_000546.6(TP53):c.7G>A (p.Glu3Lys) rs2073524362
NM_000546.6(TP53):c.83A>T (p.Glu28Val) rs786202289
NM_000546.6(TP53):c.859G>A (p.Glu287Lys) rs587782006
NM_000546.6(TP53):c.868C>G (p.Arg290Gly) rs770374782
NM_000546.6(TP53):c.873G>C (p.Lys291Asn) rs372613518
NM_000546.6(TP53):c.877G>A (p.Gly293Arg) rs587780076
NM_000546.6(TP53):c.886C>T (p.His296Tyr) rs672601296
NM_000546.6(TP53):c.892G>A (p.Glu298Lys) rs201744589
NM_000546.6(TP53):c.905G>A (p.Gly302Glu) rs1060501202
NM_000546.6(TP53):c.908G>A (p.Ser303Asn) rs876658714
NM_000546.6(TP53):c.917G>A (p.Arg306Gln) rs1048095040
NM_000546.6(TP53):c.919+3A>G rs876659784
NM_000546.6(TP53):c.920-14_920-3del rs768598540
NM_000546.6(TP53):c.924G>C (p.Leu308=) rs786202546
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.931A>C (p.Asn311His) rs1555525007
NM_000546.6(TP53):c.941C>T (p.Ser314Phe) rs751440465
NM_000546.6(TP53):c.946C>T (p.Pro316Ser) rs772773208
NM_000546.6(TP53):c.947C>T (p.Pro316Leu) rs1555524979
NM_000546.6(TP53):c.953C>T (p.Pro318Leu) rs1555524975
NM_000546.6(TP53):c.96+12G>C rs779577884
NM_000546.6(TP53):c.964C>T (p.Pro322Ser) rs863224687
NM_000546.6(TP53):c.97-3C>T rs786203749
NM_000546.6(TP53):c.97-4A>T rs746791390
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.98C>A (p.Ser33Tyr) rs1555526832
NM_000546.6(TP53):c.992A>G (p.Gln331Arg) rs1064795056
NM_000546.6(TP53):c.993+8G>A rs1060504163
NM_000546.6(TP53):c.997C>T (p.Arg333Cys) rs769934890

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