ClinVar Miner

List of variants in gene TP53 reported by Quest Diagnostics Nichols Institute San Juan Capistrano

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Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP
NM_000546.5(TP53):c.319T>C (p.Tyr107His) rs368771578
NM_000546.6(TP53):c.1040C>A (p.Ala347Asp) rs397516434
NM_000546.6(TP53):c.31G>C (p.Glu11Gln) rs201382018
NM_000546.6(TP53):c.375G>A (p.Thr125=) rs55863639
NM_000546.6(TP53):c.467G>A (p.Arg156His) rs371524413
NM_000546.6(TP53):c.586C>T (p.Arg196Ter) rs397516435
NM_000546.6(TP53):c.659A>G (p.Tyr220Cys) rs121912666
NM_000546.6(TP53):c.743G>A (p.Arg248Gln) rs11540652
NM_000546.6(TP53):c.817C>T (p.Arg273Cys) rs121913343
NM_000546.6(TP53):c.818G>A (p.Arg273His) rs28934576
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.903A>G (p.Pro301=) rs72661120
NM_000546.6(TP53):c.935C>G (p.Thr312Ser) rs145151284
NM_001126112.2(TP53):c.-5C>T rs1555527034
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.102C>G (p.Pro34=) rs11575998
NM_001126112.2(TP53):c.1079G>C (p.Gly360Ala) rs35993958
NM_001126112.2(TP53):c.1115A>C (p.Lys372Thr) rs876658876
NM_001126112.2(TP53):c.1140dup (p.Lys381Ter) rs1567540295
NM_001126112.2(TP53):c.1147C>T (p.Leu383Phe) rs150842067
NM_001126112.2(TP53):c.1151T>C (p.Met384Thr) rs1060501196
NM_001126112.2(TP53):c.11C>T (p.Pro4Leu) rs878854064
NM_001126112.2(TP53):c.123T>C (p.Asp41=) rs369129220
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.217G>A (p.Val73Met) rs587782423
NM_001126112.2(TP53):c.248C>T (p.Ala83Val) rs201717599
NM_001126112.2(TP53):c.250G>A (p.Ala84Thr) rs587781307
NM_001126112.2(TP53):c.255T>C (p.Pro85=) rs775515332
NM_001126112.2(TP53):c.271dup (p.Trp91fs) rs1597374152
NM_001126112.2(TP53):c.30C>T (p.Val10=) rs568171603
NM_001126112.2(TP53):c.329G>A (p.Arg110His) rs11540654
NM_001126112.2(TP53):c.354A>T (p.Thr118=) rs751978853
NM_001126112.2(TP53):c.374C>T (p.Thr125Met) rs786201057
NM_001126112.2(TP53):c.375+2T>C rs1555526469
NM_001126112.2(TP53):c.376-2dup rs751253294
NM_001126112.2(TP53):c.388C>G (p.Leu130Val) rs863224683
NM_001126112.2(TP53):c.460G>A (p.Gly154Ser) rs137852789
NM_001126112.2(TP53):c.464C>A (p.Thr155Asn) rs786202752
NM_001126112.2(TP53):c.464C>G (p.Thr155Ser) rs786202752
NM_001126112.2(TP53):c.472C>T (p.Arg158Cys) rs587780068
NM_001126112.2(TP53):c.489C>G (p.Tyr163Ter) rs1567553246
NM_001126112.2(TP53):c.509C>G (p.Thr170Arg) rs779000871
NM_001126112.2(TP53):c.509_512del (p.Thr170fs) rs1555526082
NM_001126112.2(TP53):c.530C>T (p.Pro177Leu) rs751477326
NM_001126112.2(TP53):c.612G>A (p.Glu204=) rs749629973
NM_001126112.2(TP53):c.617T>C (p.Leu206Ser) rs1555525804
NM_001126112.2(TP53):c.63C>T (p.Asp21=) rs1800369
NM_001126112.2(TP53):c.666G>T (p.Pro222=) rs72661118
NM_001126112.2(TP53):c.672+6G>T rs766856111
NM_001126112.2(TP53):c.694A>C (p.Ile232Leu) rs1555525562
NM_001126112.2(TP53):c.6G>A (p.Glu2=) rs143458271
NM_001126112.2(TP53):c.732C>T (p.Gly244=) rs759625762
NM_001126112.2(TP53):c.734G>A (p.Gly245Asp) rs121912656
NM_001126112.2(TP53):c.75-8del rs1567557765
NM_001126112.2(TP53):c.752T>C (p.Ile251Thr) rs730882027
NM_001126112.2(TP53):c.772G>A (p.Glu258Lys) rs121912652
NM_001126112.2(TP53):c.79C>A (p.Pro27Thr) rs922736614
NM_001126112.2(TP53):c.819T>C (p.Arg273=) rs1567547965
NM_001126112.2(TP53):c.848G>A (p.Arg283His) rs371409680
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.917G>A (p.Arg306Gln) rs1048095040
NM_001126112.2(TP53):c.924G>C (p.Leu308=) rs786202546
NM_001126112.2(TP53):c.97-9C>T rs202217267

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