ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 124
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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
NM_001126113.2(TP53):c.*1422G>C rs17883782 0.00377
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.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.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.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.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

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