ClinVar Miner

List of variants in gene TP53 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 130
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.993+12T>C rs1800899 0.01614
NM_000546.6(TP53):c.-28-341C>T rs9894227 0.01454
NM_000546.6(TP53):c.376-117G>A rs35850753 0.01358
NM_000546.6(TP53):c.639A>G (p.Arg213=) rs1800372 0.01275
NM_000546.6(TP53):c.108G>A (p.Pro36=) rs1800370 0.00974
NM_000546.6(TP53):c.-28-177G>C rs140699530 0.00930
NM_000546.6(TP53):c.1100+30A>T rs17880847 0.00929
NM_000546.6(TP53):c.376-86T>C rs113530090 0.00891
NM_000546.6(TP53):c.672+31A>G rs34949160 0.00479
NM_000546.6(TP53):c.673-100C>T rs183276131 0.00414
NC_000017.11:g.7668388C>G rs17883782 0.00377
NM_000546.6(TP53):c.*409C>A rs191918079 0.00224
NM_000546.6(TP53):c.*357T>C rs534624315 0.00197
NM_000546.6(TP53):c.994-17C>T rs368691910 0.00087
NM_000546.6(TP53):c.*1132C>T rs1044102603 0.00035
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.1014C>T (p.Phe338=) rs150293825 0.00018
NM_000546.6(TP53):c.560-8G>C rs373797299 0.00018
NM_000546.6(TP53):c.935C>G (p.Thr312Ser) rs145151284 0.00018
NM_000546.6(TP53):c.672+18G>C rs199578278 0.00014
NM_000546.6(TP53):c.869G>A (p.Arg290His) rs55819519 0.00014
NM_000546.6(TP53):c.217G>A (p.Val73Met) rs587782423 0.00011
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.474C>T (p.Arg158=) rs139200646 0.00009
NM_000546.6(TP53):c.6G>A (p.Glu2=) rs143458271 0.00009
NM_000546.6(TP53):c.847C>T (p.Arg283Cys) rs149633775 0.00009
NM_000546.6(TP53):c.993+310G>A rs201293647 0.00007
NM_000546.6(TP53):c.248C>T (p.Ala83Val) rs201717599 0.00006
NM_000546.6(TP53):c.618G>A (p.Leu206=) rs142813240 0.00006
NM_000546.6(TP53):c.920-17C>A rs911934766 0.00006
NM_000546.6(TP53):c.97-28T>A rs200989844 0.00006
NM_000546.6(TP53):c.*6T>A rs369567704 0.00005
NM_000546.6(TP53):c.102C>G (p.Pro34=) rs11575998 0.00004
NM_000546.6(TP53):c.1096T>G (p.Ser366Ala) rs17881470 0.00004
NM_000546.6(TP53):c.1149C>T (p.Leu383=) rs373710656 0.00004
NM_000546.6(TP53):c.141G>A (p.Pro47=) rs201741778 0.00004
NM_000546.6(TP53):c.246G>A (p.Pro82=) rs372397095 0.00004
NM_000546.6(TP53):c.255T>C (p.Pro85=) rs775515332 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.91G>A (p.Val31Ile) rs201753350 0.00004
NM_000546.6(TP53):c.105G>C (p.Leu35Phe) rs121912661 0.00003
NM_000546.6(TP53):c.180A>C (p.Pro60=) rs749289195 0.00003
NM_000546.6(TP53):c.188C>G (p.Ala63Gly) rs372201428 0.00003
NM_000546.6(TP53):c.30C>T (p.Val10=) rs568171603 0.00003
NM_000546.6(TP53):c.903A>G (p.Pro301=) rs72661120 0.00003
NM_000546.6(TP53):c.18A>C (p.Ser6=) rs573130482 0.00002
NM_000546.6(TP53):c.249G>A (p.Ala83=) rs55754907 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.468C>T (p.Arg156=) rs761222871 0.00002
NM_000546.6(TP53):c.510G>A (p.Thr170=) rs757544615 0.00002
NM_000546.6(TP53):c.555C>T (p.Ser185=) rs367560109 0.00002
NM_000546.6(TP53):c.612G>A (p.Glu204=) rs749629973 0.00002
NM_000546.6(TP53):c.665C>T (p.Pro222Leu) rs146340390 0.00002
NM_000546.6(TP53):c.732C>T (p.Gly244=) rs759625762 0.00002
NM_000546.6(TP53):c.1023C>T (p.Phe341=) rs864622369 0.00001
NM_000546.6(TP53):c.1025G>A (p.Arg342Gln) rs375338359 0.00001
NM_000546.6(TP53):c.1078G>A (p.Gly360Arg) rs786203298 0.00001
NM_000546.6(TP53):c.123T>C (p.Asp41=) rs369129220 0.00001
NM_000546.6(TP53):c.12G>A (p.Pro4=) rs876658274 0.00001
NM_000546.6(TP53):c.144C>T (p.Asp48=) rs587781460 0.00001
NM_000546.6(TP53):c.21T>A (p.Asp7Glu) rs587781277 0.00001
NM_000546.6(TP53):c.245C>T (p.Pro82Leu) rs534447939 0.00001
NM_000546.6(TP53):c.270C>T (p.Ser90=) rs863224370 0.00001
NM_000546.6(TP53):c.27C>T (p.Ser9=) rs757282628 0.00001
NM_000546.6(TP53):c.321C>T (p.Tyr107=) rs770776262 0.00001
NM_000546.6(TP53):c.390C>T (p.Leu130=) rs781537596 0.00001
NM_000546.6(TP53):c.45T>C (p.Ser15=) rs766765429 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.673-9del rs762540407 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.850A>T (p.Thr284Ser) rs1204379654 0.00001
NM_000546.6(TP53):c.855G>A (p.Glu285=) rs1487868349 0.00001
NM_000546.6(TP53):c.885T>C (p.Pro295=) rs200073907 0.00001
NM_000546.6(TP53):c.891C>T (p.His297=) rs750578863 0.00001
NM_000546.6(TP53):c.894G>A (p.Glu298=) rs756123992 0.00001
NM_000546.6(TP53):c.90C>T (p.Asn30=) rs370992294 0.00001
NM_000546.6(TP53):c.949C>A (p.Gln317Lys) rs764735889 0.00001
NM_000546.6(TP53):c.974G>T (p.Gly325Val) rs121912659 0.00001
NM_000546.6(TP53):c.994-5T>C rs375273756 0.00001
NM_000546.6(TP53):c.*1070C>T rs114831472
NM_000546.6(TP53):c.1015G>C (p.Glu339Gln) rs17882252
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.1131C>A (p.Thr377=) rs1456836660
NM_000546.6(TP53):c.1163A>C (p.Glu388Ala) rs587781736
NM_000546.6(TP53):c.168A>G (p.Glu56=) rs574255227
NM_000546.6(TP53):c.210T>C (p.Ala70=) rs786203513
NM_000546.6(TP53):c.264C>T (p.Ala88=) rs876660951
NM_000546.6(TP53):c.297C>T (p.Ser99=) rs751494750
NM_000546.6(TP53):c.30C>G (p.Val10=) rs568171603
NM_000546.6(TP53):c.31G>C (p.Glu11Gln) rs201382018
NM_000546.6(TP53):c.344A>G (p.His115Arg) rs730881996
NM_000546.6(TP53):c.375+17G>A rs765179201
NM_000546.6(TP53):c.376-159_376-158del rs5819162
NM_000546.6(TP53):c.456G>A (p.Pro152=) rs876659481
NM_000546.6(TP53):c.483C>A (p.Ala161=) rs1057523101
NM_000546.6(TP53):c.521G>A (p.Arg174Lys) rs1064796681
NM_000546.6(TP53):c.558T>A (p.Asp186Glu) rs375275361
NM_000546.6(TP53):c.558T>C (p.Asp186=) rs375275361
NM_000546.6(TP53):c.63C>T (p.Asp21=) rs1800369
NM_000546.6(TP53):c.666G>A (p.Pro222=) rs72661118
NM_000546.6(TP53):c.66A>G (p.Leu22=) rs748527030
NM_000546.6(TP53):c.672+48G>A rs17884607
NM_000546.6(TP53):c.672+48G>T rs17884607
NM_000546.6(TP53):c.673-19G>A rs564974117
NM_000546.6(TP53):c.673-236dup rs539331761
NM_000546.6(TP53):c.673-5C>G rs876658684
NM_000546.6(TP53):c.687T>C (p.Cys229=) rs2151022242
NM_000546.6(TP53):c.782+3C>T rs1555525425
NM_000546.6(TP53):c.787A>G (p.Asn263Asp) rs72661119
NM_000546.6(TP53):c.78T>C (p.Leu26=) rs934176141
NM_000546.6(TP53):c.843C>T (p.Asp281=) rs1057519984
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.97-11C>T rs769697802
NM_000546.6(TP53):c.97-4A>T rs746791390
NM_000546.6(TP53):c.97-52G>A rs540683791
NM_000546.6(TP53):c.993+4C>T rs1555524942
NM_000546.6(TP53):c.996C>T (p.Ile332=) rs1555524470

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.