ClinVar Miner

List of variants in gene TP53 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 115
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HGVS dbSNP
NC_000017.11:g.7674526dup
NM_000546.5(TP53):c.*13C>T rs1057520915
NM_000546.5(TP53):c.*15T>C rs374294340
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.-28-177G>C
NM_000546.5(TP53):c.1011C>T (p.Arg337=) rs1218459955
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.1065T>C (p.Ala355=) rs1057523467
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.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.1131C>A (p.Thr377=) rs1456836660
NM_000546.5(TP53):c.12G>A (p.Pro4=) rs876658274
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.210T>A (p.Ala70=) rs786203513
NM_000546.5(TP53):c.210T>C (p.Ala70=) rs786203513
NM_000546.5(TP53):c.213C>T (p.Pro71=) rs1555526701
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.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.276C>A (p.Pro92=) rs876658845
NM_000546.5(TP53):c.285T>G (p.Ser95=) rs876658696
NM_000546.5(TP53):c.30C>T (p.Val10=) rs568171603
NM_000546.5(TP53):c.319T>C (p.Tyr107His) rs368771578
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.375+13G>A rs758658664
NM_000546.5(TP53):c.375+16G>A rs750477922
NM_000546.5(TP53):c.376-117G>A
NM_000546.5(TP53):c.376-18dup rs756417643
NM_000546.5(TP53):c.376-19C>T rs1057521606
NM_000546.5(TP53):c.376-7C>T rs1555526345
NM_000546.5(TP53):c.376-86T>C
NM_000546.5(TP53):c.390C>T (p.Leu130=) rs781537596
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.471C>A (p.Val157=) rs1057522496
NM_000546.5(TP53):c.474C>T (p.Arg158=) rs139200646
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.519G>A (p.Val173=) rs1292303980
NM_000546.5(TP53):c.555C>T (p.Ser185=) rs367560109
NM_000546.5(TP53):c.558T>C (p.Asp186=) rs375275361
NM_000546.5(TP53):c.559+13G>A rs56226808
NM_000546.5(TP53):c.560-8G>C rs373797299
NM_000546.5(TP53):c.560-9del rs1555525933
NM_000546.5(TP53):c.564G>A (p.Leu188=) rs1057521837
NM_000546.5(TP53):c.612G>A (p.Glu204=) rs749629973
NM_000546.5(TP53):c.642T>G (p.His214Gln) rs587781386
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+9T>C rs1057521030
NM_000546.5(TP53):c.673-19G>A rs564974117
NM_000546.5(TP53):c.673-3T>C rs1214646363
NM_000546.5(TP53):c.673-9del rs762540407
NM_000546.5(TP53):c.678C>A (p.Gly226=) rs916168683
NM_000546.5(TP53):c.704A>G (p.Asn235Ser) rs144340710
NM_000546.5(TP53):c.732C>T (p.Gly244=) rs759625762
NM_000546.5(TP53):c.75-14C>T rs747908393
NM_000546.5(TP53):c.782+3C>T rs1555525425
NM_000546.5(TP53):c.782+6G>A rs1008479744
NM_000546.5(TP53):c.78T>C (p.Leu26=) rs934176141
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.843C>T (p.Asp281=)
NM_000546.5(TP53):c.870C>A (p.Arg290=) rs1555525135
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+13del 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+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.933C>T (p.Asn311=) rs201601993
NM_000546.5(TP53):c.93T>G (p.Val31=) rs1406108270
NM_000546.5(TP53):c.96+15T>C rs200053580
NM_000546.5(TP53):c.96+15_96+31delinsC rs1064795134
NM_000546.5(TP53):c.97-11C>T rs769697802
NM_000546.5(TP53):c.97-17T>C rs374547451
NM_000546.5(TP53):c.984C>T (p.Phe328=) rs1057520387
NM_000546.5(TP53):c.993+4C>T rs1555524942
NM_000546.5(TP53):c.994-12C>T rs1057522329
NM_000546.5(TP53):c.9G>A (p.Glu3=) rs1555527028

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