ClinVar Miner

List of variants in gene TP53 reported as uncertain significance by Color

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 192
Download table as spreadsheet
HGVS dbSNP
NC_000017.11:g.7667914C>T
NC_000017.11:g.7667923T>G
NM_000546.6(TP53):c.1093C>T (p.His365Tyr) rs267605075
NM_000546.6(TP53):c.1097C>G (p.Ser366Cys)
NM_000546.6(TP53):c.1102C>A (p.His368Asn)
NM_000546.6(TP53):c.131T>G (p.Met44Arg)
NM_000546.6(TP53):c.140C>G (p.Pro47Arg) rs1597375038
NM_000546.6(TP53):c.188C>G (p.Ala63Gly) rs372201428
NM_000546.6(TP53):c.205G>C (p.Ala69Pro)
NM_000546.6(TP53):c.253C>T (p.Pro85Ser)
NM_000546.6(TP53):c.27C>A (p.Ser9Arg) rs757282628
NM_000546.6(TP53):c.388_396dup (p.Leu130_Lys132dup)
NM_000546.6(TP53):c.467G>A (p.Arg156His) rs371524413
NM_000546.6(TP53):c.507G>T (p.Met169Ile)
NM_000546.6(TP53):c.576G>T (p.Gln192His)
NM_000546.6(TP53):c.599A>G (p.Asn200Ser)
NM_000546.6(TP53):c.5A>G (p.Glu2Gly)
NM_000546.6(TP53):c.619G>C (p.Asp207His)
NM_000546.6(TP53):c.66A>G (p.Leu22=) rs748527030
NM_000546.6(TP53):c.672+6_672+8delinsTTG
NM_000546.6(TP53):c.673-5C>T
NM_000546.6(TP53):c.684C>G (p.Asp228Glu)
NM_000546.6(TP53):c.692C>G (p.Thr231Ser)
NM_000546.6(TP53):c.74+59G>A
NM_000546.6(TP53):c.76C>A (p.Leu26Ile)
NM_000546.6(TP53):c.847C>T (p.Arg283Cys) rs149633775
NM_000546.6(TP53):c.854A>G (p.Glu285Gly)
NM_000546.6(TP53):c.85_87AAC[1] (p.Asn30del) rs587782270
NM_000546.6(TP53):c.861G>T (p.Glu287Asp)
NM_000546.6(TP53):c.86A>C (p.Asn29Thr)
NM_000546.6(TP53):c.891C>G (p.His297Gln)
NM_000546.6(TP53):c.893A>G (p.Glu298Gly)
NM_000546.6(TP53):c.944C>G (p.Ser315Cys)
NM_000546.6(TP53):c.97-3C>G
NM_000546.6(TP53):c.993+4C>G
NM_000546.6(TP53):c.997C>T (p.Arg333Cys) rs769934890
NM_001126112.2(TP53):c.1000G>C (p.Gly334Arg) rs730882028
NM_001126112.2(TP53):c.1003C>T (p.Arg335Cys) rs375444154
NM_001126112.2(TP53):c.1004G>A (p.Arg335His) rs771939956
NM_001126112.2(TP53):c.100C>A (p.Pro34Thr) rs786201968
NM_001126112.2(TP53):c.100C>G (p.Pro34Ala) rs786201968
NM_001126112.2(TP53):c.1013T>G (p.Phe338Cys) rs1064796401
NM_001126112.2(TP53):c.1014C>G (p.Phe338Leu) rs150293825
NM_001126112.2(TP53):c.1015G>C (p.Glu339Gln) rs17882252
NM_001126112.2(TP53):c.101C>G (p.Pro34Arg) rs1322947350
NM_001126112.2(TP53):c.105G>C (p.Leu35Phe) rs121912661
NM_001126112.2(TP53):c.1060C>A (p.Gln354Lys) rs755394212
NM_001126112.2(TP53):c.1061A>G (p.Gln354Arg) rs752142489
NM_001126112.2(TP53):c.1064C>T (p.Ala355Val) rs1555524382
NM_001126112.2(TP53):c.1066G>C (p.Gly356Arg) rs766786605
NM_001126112.2(TP53):c.1073A>T (p.Glu358Val) rs773553186
NM_001126112.2(TP53):c.1078G>A (p.Gly360Arg) rs786203298
NM_001126112.2(TP53):c.107C>A (p.Pro36Gln) rs587781866
NM_001126112.2(TP53):c.1081G>C (p.Gly361Arg) rs1555524361
NM_001126112.2(TP53):c.1091C>T (p.Ala364Val) rs1567541711
NM_001126112.2(TP53):c.1102C>T (p.His368Tyr) rs786204227
NM_001126112.2(TP53):c.1115A>G (p.Lys372Arg) rs876658876
NM_001126112.2(TP53):c.1118A>G (p.Lys373Arg) rs1567540504
NM_001126112.2(TP53):c.1120G>C (p.Gly374Arg) rs587781858
NM_001126112.2(TP53):c.1127C>T (p.Ser376Phe) rs1555524151
NM_001126112.2(TP53):c.1135C>A (p.Arg379Ser) rs749061599
NM_001126112.2(TP53):c.1135C>T (p.Arg379Cys) rs749061599
NM_001126112.2(TP53):c.1136G>A (p.Arg379His) rs863224682
NM_001126112.2(TP53):c.1136G>T (p.Arg379Leu) rs863224682
NM_001126112.2(TP53):c.1150A>G (p.Met384Val) rs730882009
NM_001126112.2(TP53):c.1151T>C (p.Met384Thr) rs1060501196
NM_001126112.2(TP53):c.1163A>C (p.Glu388Ala) rs587781736
NM_001126112.2(TP53):c.1173C>G (p.Asp391Glu) rs1567540133
NM_001126112.2(TP53):c.1177G>A (p.Asp393Asn) rs1192921623
NM_001126112.2(TP53):c.11C>T (p.Pro4Leu) rs878854064
NM_001126112.2(TP53):c.125A>G (p.Asp42Gly) rs587781767
NM_001126112.2(TP53):c.139C>A (p.Pro47Thr) rs1800371
NM_001126112.2(TP53):c.144C>A (p.Asp48Glu) rs587781460
NM_001126112.2(TP53):c.145G>C (p.Asp49His) rs587780728
NM_001126112.2(TP53):c.149T>A (p.Ile50Asn) rs370502517
NM_001126112.2(TP53):c.14A>G (p.Gln5Arg) rs781595324
NM_001126112.2(TP53):c.188C>T (p.Ala63Val) rs372201428
NM_001126112.2(TP53):c.19G>C (p.Asp7His) rs587782646
NM_001126112.2(TP53):c.202G>C (p.Glu68Gln) rs869312782
NM_001126112.2(TP53):c.205G>A (p.Ala69Thr) rs1567556618
NM_001126112.2(TP53):c.209C>T (p.Ala70Val) rs1567556594
NM_001126112.2(TP53):c.211C>T (p.Pro71Ser) rs1567556576
NM_001126112.2(TP53):c.214C>G (p.Pro72Ala) rs587782769
NM_001126112.2(TP53):c.214_215delinsTG (p.Pro72Cys) rs730882014
NM_001126112.2(TP53):c.215C>A (p.Pro72His) rs1042522
NM_001126112.2(TP53):c.233C>G (p.Ala78Gly) rs876658527
NM_001126112.2(TP53):c.234_263del (p.Ala79_Ala88del) rs754312472
NM_001126112.2(TP53):c.244C>G (p.Pro82Ala) rs1555526664
NM_001126112.2(TP53):c.250G>A (p.Ala84Thr) rs587781307
NM_001126112.2(TP53):c.262G>C (p.Ala88Pro) rs1567556231
NM_001126112.2(TP53):c.275C>T (p.Pro92Leu) rs1210700121
NM_001126112.2(TP53):c.28G>C (p.Val10Leu) rs535274413
NM_001126112.2(TP53):c.303A>T (p.Lys101Asn) rs878854069
NM_001126112.2(TP53):c.304A>T (p.Thr102Ser) rs1567555968
NM_001126112.2(TP53):c.305C>T (p.Thr102Ile) rs786202717
NM_001126112.2(TP53):c.317G>T (p.Ser106Ile) rs1567555883
NM_001126112.2(TP53):c.322G>A (p.Gly108Ser) rs587782461
NM_001126112.2(TP53):c.322G>C (p.Gly108Arg) rs587782461
NM_001126112.2(TP53):c.328C>T (p.Arg110Cys) rs587781371
NM_001126112.2(TP53):c.329G>A (p.Arg110His) rs11540654
NM_001126112.2(TP53):c.334G>A (p.Gly112Ser) rs1423803759
NM_001126112.2(TP53):c.341T>C (p.Leu114Ser) rs781724995
NM_001126112.2(TP53):c.344A>G (p.His115Arg) rs730881996
NM_001126112.2(TP53):c.353C>T (p.Thr118Ile) rs1064794141
NM_001126112.2(TP53):c.35C>T (p.Pro12Leu) rs1482497533
NM_001126112.2(TP53):c.364G>A (p.Val122Met) rs587781495
NM_001126112.2(TP53):c.370T>A (p.Cys124Ser) rs730881997
NM_001126112.2(TP53):c.376-2dup rs751253294
NM_001126112.2(TP53):c.37C>T (p.Pro13Ser) rs1060501208
NM_001126112.2(TP53):c.382C>A (p.Pro128Thr) rs1555526327
NM_001126112.2(TP53):c.385G>A (p.Ala129Thr) rs1438095083
NM_001126112.2(TP53):c.393C>A (p.Asn131Lys) rs769270327
NM_001126112.2(TP53):c.40C>G (p.Leu14Val) rs1567558112
NM_001126112.2(TP53):c.442G>T (p.Asp148Tyr) rs1131691007
NM_001126112.2(TP53):c.460G>A (p.Gly154Ser) rs137852789
NM_001126112.2(TP53):c.461G>A (p.Gly154Asp) rs762846821
NM_001126112.2(TP53):c.469G>A (p.Val157Ile) rs121912654
NM_001126112.2(TP53):c.472C>T (p.Arg158Cys) rs587780068
NM_001126112.2(TP53):c.480G>A (p.Met160Ile) rs772354334
NM_001126112.2(TP53):c.481G>A (p.Ala161Thr) rs193920817
NM_001126112.2(TP53):c.4G>A (p.Glu2Lys) rs769884991
NM_001126112.2(TP53):c.500A>C (p.Gln167Pro) rs1319163924
NM_001126112.2(TP53):c.509C>G (p.Thr170Arg) rs779000871
NM_001126112.2(TP53):c.509C>T (p.Thr170Met) rs779000871
NM_001126112.2(TP53):c.536A>G (p.His179Arg) rs1057519991
NM_001126112.2(TP53):c.541C>A (p.Arg181Ser) rs587782596
NM_001126112.2(TP53):c.541C>T (p.Arg181Cys) rs587782596
NM_001126112.2(TP53):c.554G>A (p.Ser185Asn) rs150607408
NM_001126112.2(TP53):c.559+5G>A rs1555525956
NM_001126112.2(TP53):c.560-12G>A rs1567552329
NM_001126112.2(TP53):c.566C>T (p.Ala189Val) rs121912665
NM_001126112.2(TP53):c.572C>G (p.Pro191Arg) rs587778718
NM_001126112.2(TP53):c.584T>G (p.Ile195Ser) rs760043106
NM_001126112.2(TP53):c.587G>A (p.Arg196Gln) rs483352697
NM_001126112.2(TP53):c.587G>C (p.Arg196Pro) rs483352697
NM_001126112.2(TP53):c.604C>G (p.Arg202Gly) rs587780072
NM_001126112.2(TP53):c.604C>T (p.Arg202Cys) rs587780072
NM_001126112.2(TP53):c.605G>A (p.Arg202His) rs587778719
NM_001126112.2(TP53):c.613T>C (p.Tyr205His) rs1057520008
NM_001126112.2(TP53):c.625A>G (p.Arg209Gly) rs1429743956
NM_001126112.2(TP53):c.634T>A (p.Phe212Ile) rs1064795766
NM_001126112.2(TP53):c.643A>G (p.Ser215Gly) rs886039484
NM_001126112.2(TP53):c.653T>G (p.Val218Gly) rs1555525743
NM_001126112.2(TP53):c.661G>A (p.Glu221Lys) rs786201592
NM_001126112.2(TP53):c.665C>T (p.Pro222Leu) rs146340390
NM_001126112.2(TP53):c.673-4C>G rs1555525586
NM_001126112.2(TP53):c.673-5C>G rs876658684
NM_001126112.2(TP53):c.677G>T (p.Gly226Val) rs970212462
NM_001126112.2(TP53):c.686G>A (p.Cys229Tyr) rs1064793603
NM_001126112.2(TP53):c.747G>T (p.Arg249Ser) rs28934571
NM_001126112.2(TP53):c.760A>G (p.Ile254Val) rs746601313
NM_001126112.2(TP53):c.776A>G (p.Asp259Gly) rs745425759
NM_001126112.2(TP53):c.779C>A (p.Ser260Tyr) rs876658916
NM_001126112.2(TP53):c.782+6G>A rs1008479744
NM_001126112.2(TP53):c.783-10T>C rs377590379
NM_001126112.2(TP53):c.784G>A (p.Gly262Ser) rs200579969
NM_001126112.2(TP53):c.79C>T (p.Pro27Ser) rs922736614
NM_001126112.2(TP53):c.800G>A (p.Arg267Gln) rs587780075
NM_001126112.2(TP53):c.811G>A (p.Glu271Lys) rs1060501191
NM_001126112.2(TP53):c.824G>C (p.Cys275Ser) rs863224451
NM_001126112.2(TP53):c.845G>A (p.Arg282Gln) rs730882008
NM_001126112.2(TP53):c.848G>A (p.Arg283His) rs371409680
NM_001126112.2(TP53):c.850A>T (p.Thr284Ser) rs1204379654
NM_001126112.2(TP53):c.851C>T (p.Thr284Ile) rs863224685
NM_001126112.2(TP53):c.861G>C (p.Glu287Asp) rs748891343
NM_001126112.2(TP53):c.868C>G (p.Arg290Gly) rs770374782
NM_001126112.2(TP53):c.868C>T (p.Arg290Cys) rs770374782
NM_001126112.2(TP53):c.873G>C (p.Lys291Asn) rs372613518
NM_001126112.2(TP53):c.875A>G (p.Lys292Arg) rs121912663
NM_001126112.2(TP53):c.877G>A (p.Gly293Arg) rs587780076
NM_001126112.2(TP53):c.877G>T (p.Gly293Trp) rs587780076
NM_001126112.2(TP53):c.884C>T (p.Pro295Leu) rs751713111
NM_001126112.2(TP53):c.886C>T (p.His296Tyr) rs672601296
NM_001126112.2(TP53):c.892G>A (p.Glu298Lys) rs201744589
NM_001126112.2(TP53):c.907A>G (p.Ser303Gly) rs587782391
NM_001126112.2(TP53):c.910A>G (p.Thr304Ala) rs587782654
NM_001126112.2(TP53):c.917G>A (p.Arg306Gln) rs1048095040
NM_001126112.2(TP53):c.919+3A>G rs876659784
NM_001126112.2(TP53):c.920-3T>C rs1367689213
NM_001126112.2(TP53):c.925C>T (p.Pro309Ser) rs1555525012
NM_001126112.2(TP53):c.943T>A (p.Ser315Thr) rs762620193
NM_001126112.2(TP53):c.949C>A (p.Gln317Lys) rs764735889
NM_001126112.2(TP53):c.953C>T (p.Pro318Leu) rs1555524975
NM_001126112.2(TP53):c.97-3C>T rs786203749
NM_001126112.2(TP53):c.97-4A>T rs746791390
NM_001126112.2(TP53):c.970G>C (p.Asp324His) rs1064794810
NM_001126112.2(TP53):c.970G>T (p.Asp324Tyr) rs1064794810
NM_001126112.2(TP53):c.974G>A (p.Gly325Glu) rs121912659
NM_001126112.2(TP53):c.974G>T (p.Gly325Val) rs121912659
NM_001126112.2(TP53):c.986C>T (p.Thr329Ile) rs969930693
NM_001126112.2(TP53):c.993+4C>T rs1555524942
NM_001126112.2(TP53):c.998G>A (p.Arg333His) rs573154688

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.