ClinVar Miner

List of variants in gene TP53 studied for not specified

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Gene type:
ClinVar version:
Total variants: 214
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HGVS dbSNP
NM_000546.5(TP53):c.*13C>T rs1057520915
NM_000546.5(TP53):c.*15T>C rs374294340
NM_000546.5(TP53):c.*16G>T rs879254030
NM_000546.5(TP53):c.*6T>A rs369567704
NM_000546.5(TP53):c.-11G>A rs773666793
NM_000546.5(TP53):c.-12C>T rs375229869
NM_000546.5(TP53):c.-16C>T rs1057520385
NM_000546.5(TP53):c.-20C>G rs1057522035
NM_000546.5(TP53):c.-28-14T>G rs1555527049
NM_000546.5(TP53):c.-5C>T rs1555527034
NM_000546.5(TP53):c.1011C>G (p.Arg337=) rs1218459955
NM_000546.5(TP53):c.1011C>T (p.Arg337=) rs1218459955
NM_000546.5(TP53):c.1014C>T (p.Phe338=) rs150293825
NM_000546.5(TP53):c.1015G>A (p.Glu339Lys) rs17882252
NM_000546.5(TP53):c.1023C>T (p.Phe341=) rs864622369
NM_000546.5(TP53):c.102C>G (p.Pro34=) rs11575998
NM_000546.5(TP53):c.1040C>A (p.Ala347Asp) rs397516434
NM_000546.5(TP53):c.1065T>C (p.Ala355=) rs1057523467
NM_000546.5(TP53):c.1066G>C (p.Gly356Arg) rs766786605
NM_000546.5(TP53):c.1073A>T (p.Glu358Val) rs773553186
NM_000546.5(TP53):c.1079G>C (p.Gly360Ala) rs35993958
NM_000546.5(TP53):c.1079G>T (p.Gly360Val) rs35993958
NM_000546.5(TP53):c.1082G>A (p.Gly361Glu) rs587781663
NM_000546.5(TP53):c.1083G>A (p.Gly361=) rs886038349
NM_000546.5(TP53):c.108G>A (p.Pro36=) rs1800370
NM_000546.5(TP53):c.1096T>G (p.Ser366Ala) rs17881470
NM_000546.5(TP53):c.1100+14_1100+20del rs1555524330
NM_000546.5(TP53):c.1100+16C>T rs1056928992
NM_000546.5(TP53):c.1100+3G>C rs1057521454
NM_000546.5(TP53):c.1100+8A>G rs878854062
NM_000546.5(TP53):c.1101-3C>T rs1057521167
NM_000546.5(TP53):c.1115A>C (p.Lys372Thr) rs876658876
NM_000546.5(TP53):c.1131C>A (p.Thr377=) rs1456836660
NM_000546.5(TP53):c.1150A>G (p.Met384Val) rs730882009
NM_000546.5(TP53):c.1151_1153delinsG (p.Met384fs) rs1064793281
NM_000546.5(TP53):c.11C>T (p.Pro4Leu) rs878854064
NM_000546.5(TP53):c.12G>A (p.Pro4=) rs876658274
NM_000546.5(TP53):c.139C>T (p.Pro47Ser) rs1800371
NM_000546.5(TP53):c.141G>A (p.Pro47=) rs201741778
NM_000546.5(TP53):c.145G>A (p.Asp49Asn) rs587780728
NM_000546.5(TP53):c.156A>G (p.Gln52=) rs1057523702
NM_000546.5(TP53):c.173C>G (p.Pro58Arg) rs144386518
NM_000546.5(TP53):c.180A>C (p.Pro60=) rs749289195
NM_000546.5(TP53):c.185_232del (p.Glu62_Pro77del) rs1567556432
NM_000546.5(TP53):c.188C>G (p.Ala63Gly) rs372201428
NM_000546.5(TP53):c.18A>C (p.Ser6=) rs573130482
NM_000546.5(TP53):c.210T>A (p.Ala70=) rs786203513
NM_000546.5(TP53):c.213C>T (p.Pro71=) rs1555526701
NM_000546.5(TP53):c.215= (p.Pro72=) rs1042522
NM_000546.5(TP53):c.215C>G (p.Pro72Arg) rs1042522
NM_000546.5(TP53):c.215_216delinsGT (p.Pro72Arg) rs878854066
NM_000546.5(TP53):c.216C>T (p.Pro72=) rs56275308
NM_000546.5(TP53):c.21T>A (p.Asp7Glu) rs587781277
NM_000546.5(TP53):c.222C>T (p.Ala74=) rs786201577
NM_000546.5(TP53):c.234A>G (p.Ala78=) rs375099397
NM_000546.5(TP53):c.246G>A (p.Pro82=) rs372397095
NM_000546.5(TP53):c.248C>T (p.Ala83Val) rs201717599
NM_000546.5(TP53):c.249G>A (p.Ala83=) rs55754907
NM_000546.5(TP53):c.255T>C (p.Pro85=) rs775515332
NM_000546.5(TP53):c.267C>A (p.Pro89=) rs786201443
NM_000546.5(TP53):c.267C>T (p.Pro89=) rs786201443
NM_000546.5(TP53):c.270C>T (p.Ser90=) rs863224370
NM_000546.5(TP53):c.276C>A (p.Pro92=) rs876658845
NM_000546.5(TP53):c.285T>G (p.Ser95=) rs876658696
NM_000546.5(TP53):c.28G>A (p.Val10Ile) rs535274413
NM_000546.5(TP53):c.30C>T (p.Val10=) rs568171603
NM_000546.5(TP53):c.318C>G (p.Ser106Arg) rs1555526581
NM_000546.5(TP53):c.319T>C (p.Tyr107His) rs368771578
NM_000546.5(TP53):c.31G>A (p.Glu11Lys) rs201382018
NM_000546.5(TP53):c.31G>C (p.Glu11Gln) rs201382018
NM_000546.5(TP53):c.321C>T (p.Tyr107=) rs770776262
NM_000546.5(TP53):c.326T>C (p.Phe109Ser) rs1064796722
NM_000546.5(TP53):c.328C>T (p.Arg110Cys) rs587781371
NM_000546.5(TP53):c.329G>A (p.Arg110His) rs11540654
NM_000546.5(TP53):c.354A>T (p.Thr118=) rs751978853
NM_000546.5(TP53):c.364G>A (p.Val122Met) rs587781495
NM_000546.5(TP53):c.375+13G>A rs758658664
NM_000546.5(TP53):c.375+16G>A rs750477922
NM_000546.5(TP53):c.375+5_375+11del rs730882021
NM_000546.5(TP53):c.376-17C>T rs376713749
NM_000546.5(TP53):c.376-18dupT rs756417643
NM_000546.5(TP53):c.376-19C>T rs1057521606
NM_000546.5(TP53):c.376-2dupA rs751253294
NM_000546.5(TP53):c.376-7C>T rs1555526345
NM_000546.5(TP53):c.376-91G>A rs2909430
NM_000546.5(TP53):c.380C>T (p.Ser127Phe) rs730881999
NM_000546.5(TP53):c.390C>T (p.Leu130=) rs781537596
NM_000546.5(TP53):c.390_392CAA[1] (p.Asn131del) rs879254214
NM_000546.5(TP53):c.408A>G (p.Gln136=) rs758781593
NM_000546.5(TP53):c.450A>C (p.Thr150=) rs754020850
NM_000546.5(TP53):c.450A>G (p.Thr150=) rs754020850
NM_000546.5(TP53):c.456G>A (p.Pro152=) rs876659481
NM_000546.5(TP53):c.459C>T (p.Pro153=) rs72661116
NM_000546.5(TP53):c.464C>A (p.Thr155Asn) rs786202752
NM_000546.5(TP53):c.467G>A (p.Arg156His) rs371524413
NM_000546.5(TP53):c.468C>T (p.Arg156=) rs761222871
NM_000546.5(TP53):c.471C>A (p.Val157=) rs1057522496
NM_000546.5(TP53):c.474C>T (p.Arg158=) rs139200646
NM_000546.5(TP53):c.475G>C (p.Ala159Pro) rs730882000
NM_000546.5(TP53):c.475_476delinsTT (p.Ala159Phe) rs730882022
NM_000546.5(TP53):c.477C>T (p.Ala159=) rs1057521842
NM_000546.5(TP53):c.483C>A (p.Ala161=) rs1057523101
NM_000546.5(TP53):c.504C>T (p.His168=) rs746293837
NM_000546.5(TP53):c.510G>A (p.Thr170=) rs757544615
NM_000546.5(TP53):c.518T>A (p.Val173Glu) rs1057519747
NM_000546.5(TP53):c.519G>A (p.Val173=) rs1292303980
NM_000546.5(TP53):c.555C>T (p.Ser185=) rs367560109
NM_000546.5(TP53):c.557_559+2delinsGGGG rs1567552467
NM_000546.5(TP53):c.558T>C (p.Asp186=) rs375275361
NM_000546.5(TP53):c.559+13G>A rs56226808
NM_000546.5(TP53):c.559+24C>T rs56181208
NM_000546.5(TP53):c.559+2del rs1567552459
NM_000546.5(TP53):c.559+8G>A rs775915220
NM_000546.5(TP53):c.560-8G>C rs373797299
NM_000546.5(TP53):c.560-9delT rs1555525933
NM_000546.5(TP53):c.564G>A (p.Leu188=) rs1057521837
NM_000546.5(TP53):c.572C>G (p.Pro191Arg) rs587778718
NM_000546.5(TP53):c.582T>C (p.Leu194=) rs370216745
NM_000546.5(TP53):c.605G>A (p.Arg202His) rs587778719
NM_000546.5(TP53):c.612G>A (p.Glu204=) rs749629973
NM_000546.5(TP53):c.617T>C (p.Leu206Ser) rs1555525804
NM_000546.5(TP53):c.637C>T (p.Arg213Ter) rs397516436
NM_000546.5(TP53):c.638G>A (p.Arg213Gln) rs587778720
NM_000546.5(TP53):c.638G>C (p.Arg213Pro) rs587778720
NM_000546.5(TP53):c.639A>G (p.Arg213=) rs1800372
NM_000546.5(TP53):c.63C>T (p.Asp21=) rs1800369
NM_000546.5(TP53):c.642T>G (p.His214Gln) rs587781386
NM_000546.5(TP53):c.646G>A (p.Val216Met) rs730882025
NM_000546.5(TP53):c.655C>T (p.Pro219Ser) rs879253894
NM_000546.5(TP53):c.666G>A (p.Pro222=) rs72661118
NM_000546.5(TP53):c.672+14C>G rs1555525697
NM_000546.5(TP53):c.672+15T>C rs140756213
NM_000546.5(TP53):c.672+15T>G rs140756213
NM_000546.5(TP53):c.672+18G>C rs199578278
NM_000546.5(TP53):c.672+31A>G rs34949160
NM_000546.5(TP53):c.672+35G>T rs587778001
NM_000546.5(TP53):c.672+62A>G rs1625895
NM_000546.5(TP53):c.672+9T>C rs1057521030
NM_000546.5(TP53):c.673-19G>A rs564974117
NM_000546.5(TP53):c.673-36G>C rs17880604
NM_000546.5(TP53):c.673-3T>C rs1214646363
NM_000546.5(TP53):c.673-9delA rs762540407
NM_000546.5(TP53):c.678C>A (p.Gly226=) rs916168683
NM_000546.5(TP53):c.695T>C (p.Ile232Thr) rs587781589
NM_000546.5(TP53):c.6G>A (p.Glu2=) rs143458271
NM_000546.5(TP53):c.704A>G (p.Asn235Ser) rs144340710
NM_000546.5(TP53):c.709A>G (p.Met237Val) rs730882004
NM_000546.5(TP53):c.711G>A (p.Met237Ile) rs587782664
NM_000546.5(TP53):c.718_741del (p.Ser240_Asn247del) rs397516437
NM_000546.5(TP53):c.732C>T (p.Gly244=) rs759625762
NM_000546.5(TP53):c.74+14T>C rs184743157
NM_000546.5(TP53):c.74+38C>G rs1642785
NM_000546.5(TP53):c.75-14C>T rs747908393
NM_000546.5(TP53):c.752T>C (p.Ile251Thr) rs730882027
NM_000546.5(TP53):c.758C>A (p.Thr253Asn) rs1555525465
NM_000546.5(TP53):c.769C>T (p.Leu257=) rs779761818
NM_000546.5(TP53):c.772G>A (p.Glu258Lys) rs121912652
NM_000546.5(TP53):c.782+10C>T rs200277687
NM_000546.5(TP53):c.782+12C>T rs17881780
NM_000546.5(TP53):c.782+17C>T rs17880172
NM_000546.5(TP53):c.782+6G>A rs1008479744
NM_000546.5(TP53):c.790del (p.Leu264fs) rs1060501194
NM_000546.5(TP53):c.818G>A (p.Arg273His) rs28934576
NM_000546.5(TP53):c.81T>C (p.Pro27=) rs1555526932
NM_000546.5(TP53):c.831T>C (p.Cys277=) rs1057523347
NM_000546.5(TP53):c.836G>A (p.Gly279Glu) rs1064793881
NM_000546.5(TP53):c.845G>A (p.Arg282Gln) rs730882008
NM_000546.5(TP53):c.847C>T (p.Arg283Cys) rs149633775
NM_000546.5(TP53):c.848G>A (p.Arg283His) rs371409680
NM_000546.5(TP53):c.85_87AAC[1] (p.Asn30del) rs587782270
NM_000546.5(TP53):c.869G>A (p.Arg290His) rs55819519
NM_000546.5(TP53):c.869G>T (p.Arg290Leu) rs55819519
NM_000546.5(TP53):c.870C>A (p.Arg290=) rs1555525135
NM_000546.5(TP53):c.885T>C (p.Pro295=) rs200073907
NM_000546.5(TP53):c.891C>T (p.His297=) rs750578863
NM_000546.5(TP53):c.900C>G (p.Pro300=) rs767356182
NM_000546.5(TP53):c.903A>G (p.Pro301=) rs72661120
NM_000546.5(TP53):c.90C>T (p.Asn30=) rs370992294
NM_000546.5(TP53):c.919+13delG rs936119541
NM_000546.5(TP53):c.919+15C>G rs1057523528
NM_000546.5(TP53):c.919+17A>G rs1057520386
NM_000546.5(TP53):c.919+19_919+21del rs1064794839
NM_000546.5(TP53):c.919+5G>T rs766127339
NM_000546.5(TP53):c.919+7A>C rs199527475
NM_000546.5(TP53):c.919+9G>A rs772829199
NM_000546.5(TP53):c.91G>A (p.Val31Ile) rs201753350
NM_000546.5(TP53):c.920-11C>T rs1057523270
NM_000546.5(TP53):c.920-13G>C rs1057522354
NM_000546.5(TP53):c.920-14T>C rs752627700
NM_000546.5(TP53):c.924G>A (p.Leu308=) rs786202546
NM_000546.5(TP53):c.924G>C (p.Leu308=) rs786202546
NM_000546.5(TP53):c.933C>T (p.Asn311=) rs201601993
NM_000546.5(TP53):c.93T>G (p.Val31=) rs1406108270
NM_000546.5(TP53):c.96+14T>C rs757865517
NM_000546.5(TP53):c.96+15T>C rs200053580
NM_000546.5(TP53):c.96+15_96+31delinsC rs1064795134
NM_000546.5(TP53):c.96+16_96+31del16 rs59758982
NM_000546.5(TP53):c.96+41_97-54dup rs59758982
NM_000546.5(TP53):c.97-11C>T rs769697802
NM_000546.5(TP53):c.97-17T>C rs374547451
NM_000546.5(TP53):c.97-29C>A rs17883323
NM_000546.5(TP53):c.97-6C>T rs35117667
NM_000546.5(TP53):c.97-9C>T rs202217267
NM_000546.5(TP53):c.974G>T (p.Gly325Val) rs121912659
NM_000546.5(TP53):c.984C>T (p.Phe328=) rs1057520387
NM_000546.5(TP53):c.993+12T>C rs1800899
NM_000546.5(TP53):c.993+13G>C rs369599972
NM_000546.5(TP53):c.993+4C>T rs1555524942
NM_000546.5(TP53):c.994-12C>T rs1057522329
NM_000546.5(TP53):c.994-17C>T rs368691910
NM_000546.5(TP53):c.997C>T (p.Arg333Cys) rs769934890
NM_000546.5(TP53):c.9G>A (p.Glu3=) rs1555527028
NM_001126113.2(TP53):c.1034C>T (p.Ser345Leu) rs758194998
NM_001126114.2(TP53):c.1021T>G (p.Cys341Gly) rs3021068

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