ClinVar Miner

List of variants in gene TP53 reported as likely benign for adrenal gland disease

Included ClinVar conditions (131):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 161
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HGVS dbSNP
NM_000546.5(TP53):c.319T>C (p.Tyr107His) rs368771578
NM_000546.6(TP53):c.*357T>C
NM_000546.6(TP53):c.*409C>A
NM_000546.6(TP53):c.1093C>T (p.His365Tyr) rs267605075
NM_000546.6(TP53):c.28G>A (p.Val10Ile) rs535274413
NM_000546.6(TP53):c.467G>A (p.Arg156His) rs371524413
NM_000546.6(TP53):c.642T>G (p.His214Gln) rs587781386
NM_000546.6(TP53):c.66A>G (p.Leu22=) rs748527030
NM_000546.6(TP53):c.844C>T (p.Arg282Trp) rs28934574
NM_000546.6(TP53):c.847C>T (p.Arg283Cys) rs149633775
NM_000546.6(TP53):c.869G>A (p.Arg290His) rs55819519
NM_000546.6(TP53):c.885T>C (p.Pro295=) rs200073907
NM_000546.6(TP53):c.91G>A (p.Val31Ile) rs201753350
NM_000546.6(TP53):c.935C>G (p.Thr312Ser) rs145151284
NM_001126112.2(TP53):c.*569_*570del rs1555523911
NM_001126112.2(TP53):c.*936A>G rs55817367
NM_001126112.2(TP53):c.1002G>A (p.Gly334=) rs786203531
NM_001126112.2(TP53):c.1014C>T (p.Phe338=) rs150293825
NM_001126112.2(TP53):c.1015G>A (p.Glu339Lys) rs17882252
NM_001126112.2(TP53):c.1023C>T (p.Phe341=) rs864622369
NM_001126112.2(TP53):c.102C>G (p.Pro34=) rs11575998
NM_001126112.2(TP53):c.1032G>A (p.Leu344=) rs752189180
NM_001126112.2(TP53):c.1032G>C (p.Leu344=) rs752189180
NM_001126112.2(TP53):c.1041C>G (p.Ala347=) rs1450229137
NM_001126112.2(TP53):c.1079G>C (p.Gly360Ala) rs35993958
NM_001126112.2(TP53):c.1096T>G (p.Ser366Ala) rs17881470
NM_001126112.2(TP53):c.1100+10C>T rs374041625
NM_001126112.2(TP53):c.1100+7G>A rs777374791
NM_001126112.2(TP53):c.1100+8A>G rs878854062
NM_001126112.2(TP53):c.1119G>A (p.Lys373=) rs1342613419
NM_001126112.2(TP53):c.111C>T (p.Ser37=) rs1555526798
NM_001126112.2(TP53):c.1120G>C (p.Gly374Arg) rs587781858
NM_001126112.2(TP53):c.1131C>A (p.Thr377=) rs1456836660
NM_001126112.2(TP53):c.1131C>T (p.Thr377=) rs1456836660
NM_001126112.2(TP53):c.1149C>T (p.Leu383=) rs373710656
NM_001126112.2(TP53):c.12G>A (p.Pro4=) rs876658274
NM_001126112.2(TP53):c.135G>A (p.Leu45=) rs1060504164
NM_001126112.2(TP53):c.144C>T (p.Asp48=) rs587781460
NM_001126112.2(TP53):c.145G>A (p.Asp49Asn) rs587780728
NM_001126112.2(TP53):c.147T>C (p.Asp49=) rs786201148
NM_001126112.2(TP53):c.173C>G (p.Pro58Arg) rs144386518
NM_001126112.2(TP53):c.180A>C (p.Pro60=) rs749289195
NM_001126112.2(TP53):c.18A>C (p.Ser6=) rs573130482
NM_001126112.2(TP53):c.18A>G (p.Ser6=) rs573130482
NM_001126112.2(TP53):c.192C>G (p.Pro64=) rs1555526723
NM_001126112.2(TP53):c.207T>C (p.Ala69=) rs775185978
NM_001126112.2(TP53):c.210T>A (p.Ala70=) rs786203513
NM_001126112.2(TP53):c.210T>C (p.Ala70=) rs786203513
NM_001126112.2(TP53):c.215_216delinsGT (p.Pro72Arg) rs878854066
NM_001126112.2(TP53):c.216C>T (p.Pro72=) rs56275308
NM_001126112.2(TP53):c.21T>A (p.Asp7Glu) rs587781277
NM_001126112.2(TP53):c.222C>T (p.Ala74=) rs786201577
NM_001126112.2(TP53):c.234A>G (p.Ala78=) rs375099397
NM_001126112.2(TP53):c.245C>T (p.Pro82Leu) rs534447939
NM_001126112.2(TP53):c.246G>A (p.Pro82=) rs372397095
NM_001126112.2(TP53):c.248C>T (p.Ala83Val) rs201717599
NM_001126112.2(TP53):c.249G>A (p.Ala83=) rs55754907
NM_001126112.2(TP53):c.255T>C (p.Pro85=) rs775515332
NM_001126112.2(TP53):c.264C>T (p.Ala88=) rs876660951
NM_001126112.2(TP53):c.267C>T (p.Pro89=) rs786201443
NM_001126112.2(TP53):c.270C>T (p.Ser90=) rs863224370
NM_001126112.2(TP53):c.279G>T (p.Leu93=) rs878854067
NM_001126112.2(TP53):c.27C>T (p.Ser9=) rs757282628
NM_001126112.2(TP53):c.282A>G (p.Ser94=) rs771721337
NM_001126112.2(TP53):c.297C>T (p.Ser99=) rs751494750
NM_001126112.2(TP53):c.30C>G (p.Val10=) rs568171603
NM_001126112.2(TP53):c.30C>T (p.Val10=) rs568171603
NM_001126112.2(TP53):c.331C>T (p.Leu111=) rs1403707528
NM_001126112.2(TP53):c.351G>A (p.Gly117=) rs876658998
NM_001126112.2(TP53):c.354A>T (p.Thr118=) rs751978853
NM_001126112.2(TP53):c.375+17G>A rs765179201
NM_001126112.2(TP53):c.375+8G>T rs1597373333
NM_001126112.2(TP53):c.376-18dup rs756417643
NM_001126112.2(TP53):c.376-7C>T rs1555526345
NM_001126112.2(TP53):c.390C>T (p.Leu130=) rs781537596
NM_001126112.2(TP53):c.408A>G (p.Gln136=) rs758781593
NM_001126112.2(TP53):c.450A>G (p.Thr150=) rs754020850
NM_001126112.2(TP53):c.456G>A (p.Pro152=) rs876659481
NM_001126112.2(TP53):c.459C>T (p.Pro153=) rs72661116
NM_001126112.2(TP53):c.45T>C (p.Ser15=) rs766765429
NM_001126112.2(TP53):c.465C>A (p.Thr155=) rs786202992
NM_001126112.2(TP53):c.468C>T (p.Arg156=) rs761222871
NM_001126112.2(TP53):c.474C>T (p.Arg158=) rs139200646
NM_001126112.2(TP53):c.483C>A (p.Ala161=) rs1057523101
NM_001126112.2(TP53):c.498A>G (p.Ser166=) rs1555526098
NM_001126112.2(TP53):c.510G>A (p.Thr170=) rs757544615
NM_001126112.2(TP53):c.54A>G (p.Thr18=) rs876659984
NM_001126112.2(TP53):c.555C>T (p.Ser185=) rs367560109
NM_001126112.2(TP53):c.558T>C (p.Asp186=) rs375275361
NM_001126112.2(TP53):c.559+8G>A rs775915220
NM_001126112.2(TP53):c.560-11_560-8dup rs1555525931
NM_001126112.2(TP53):c.560-6T>C rs1555525929
NM_001126112.2(TP53):c.582T>C (p.Leu194=) rs370216745
NM_001126112.2(TP53):c.606T>C (p.Arg202=) rs1392931620
NM_001126112.2(TP53):c.612G>A (p.Glu204=) rs749629973
NM_001126112.2(TP53):c.615T>C (p.Tyr205=) rs786202222
NM_001126112.2(TP53):c.616T>C (p.Leu206=) rs1597368418
NM_001126112.2(TP53):c.618G>A (p.Leu206=) rs142813240
NM_001126112.2(TP53):c.642T>C (p.His214=) rs587781386
NM_001126112.2(TP53):c.657C>A (p.Pro219=) rs786201859
NM_001126112.2(TP53):c.665C>T (p.Pro222Leu) rs146340390
NM_001126112.2(TP53):c.666G>A (p.Pro222=) rs72661118
NM_001126112.2(TP53):c.666G>T (p.Pro222=) rs72661118
NM_001126112.2(TP53):c.672+15T>C rs140756213
NM_001126112.2(TP53):c.672+18G>C rs199578278
NM_001126112.2(TP53):c.673-37C>T rs374907737
NM_001126112.2(TP53):c.673-9del rs762540407
NM_001126112.2(TP53):c.6G>A (p.Glu2=) rs143458271
NM_001126112.2(TP53):c.704A>G (p.Asn235Ser) rs144340710
NM_001126112.2(TP53):c.732C>T (p.Gly244=) rs759625762
NM_001126112.2(TP53):c.74+14T>C rs184743157
NM_001126112.2(TP53):c.74+7G>T rs1597376387
NM_001126112.2(TP53):c.74+8G>A rs776933919
NM_001126112.2(TP53):c.74+9A>C rs1057517593
NM_001126112.2(TP53):c.741C>T (p.Asn247=) rs786202448
NM_001126112.2(TP53):c.75-8T>C rs1555526938
NM_001126112.2(TP53):c.753C>T (p.Ile251=) rs878854074
NM_001126112.2(TP53):c.768A>G (p.Thr256=) rs786203563
NM_001126112.2(TP53):c.769C>T (p.Leu257=) rs779761818
NM_001126112.2(TP53):c.782+10C>T rs200277687
NM_001126112.2(TP53):c.782+12C>T rs17881780
NM_001126112.2(TP53):c.783-10T>C rs377590379
NM_001126112.2(TP53):c.783-13C>G rs1555525373
NM_001126112.2(TP53):c.783-4G>A rs1060504160
NM_001126112.2(TP53):c.787A>G (p.Asn263Asp) rs72661119
NM_001126112.2(TP53):c.849C>G (p.Arg283=) rs1555525197
NM_001126112.2(TP53):c.867C>T (p.Leu289=) rs778138282
NM_001126112.2(TP53):c.891C>T (p.His297=) rs750578863
NM_001126112.2(TP53):c.892G>A (p.Glu298Lys) rs201744589
NM_001126112.2(TP53):c.894G>A (p.Glu298=) rs756123992
NM_001126112.2(TP53):c.90C>T (p.Asn30=) rs370992294
NM_001126112.2(TP53):c.916C>A (p.Arg306=) rs121913344
NM_001126112.2(TP53):c.917G>A (p.Arg306Gln) rs1048095040
NM_001126112.2(TP53):c.919+7A>C rs199527475
NM_001126112.2(TP53):c.919+8A>C rs1555525043
NM_001126112.2(TP53):c.919+9G>A rs772829199
NM_001126112.2(TP53):c.920-4C>G rs1555525022
NM_001126112.2(TP53):c.920-5C>A rs34361146
NM_001126112.2(TP53):c.920-5C>T rs34361146
NM_001126112.2(TP53):c.920-8T>C rs1555525024
NM_001126112.2(TP53):c.924G>A (p.Leu308=) rs786202546
NM_001126112.2(TP53):c.924G>C (p.Leu308=) rs786202546
NM_001126112.2(TP53):c.936C>G (p.Thr312=) rs1555524991
NM_001126112.2(TP53):c.942C>A (p.Ser314=) rs765930028
NM_001126112.2(TP53):c.97-15T>C rs1555526843
NM_001126112.2(TP53):c.97-28T>A rs200989844
NM_001126112.2(TP53):c.97-4A>T rs746791390
NM_001126112.2(TP53):c.97-9C>T rs202217267
NM_001126112.2(TP53):c.975A>G (p.Gly325=) rs1245012034
NM_001126112.2(TP53):c.993+234G>A rs17883348
NM_001126112.2(TP53):c.993+244G>A rs576532147
NM_001126112.2(TP53):c.993+326_993+341del rs730882013
NM_001126112.2(TP53):c.993+8G>A rs1060504163
NM_001126112.2(TP53):c.994-17C>T rs368691910
NM_001126112.2(TP53):c.994-5T>C rs375273756
NM_001126112.2(TP53):c.994-6C>A rs1555524474
NM_001126113.2(TP53):c.*1422G>C rs17883782
NM_001126113.2(TP53):c.1015T>C (p.Cys339Arg) rs1642789
NM_001126113.2(TP53):c.1034_1036CGT[1] (p.Ser346del) rs1555524872
NM_001126114.2(TP53):c.1021T>G (p.Cys341Gly) rs3021068
NM_001126114.2(TP53):c.1025A>C (p.Ter342Ser) rs764562217

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