ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.376-283T>C rs1794287 0.84958
NM_000546.6(TP53):c.376-91G>A rs2909430 0.83528
NM_000546.6(TP53):c.672+62A>G rs1625895 0.83418
NM_000546.6(TP53):c.74+38C>G rs1642785 0.66254
NM_000546.6(TP53):c.215C>G (p.Pro72Arg) rs1042522 0.62654
NC_000017.11:g.7668134G>A rs1614984 0.40219
NM_000546.6(TP53):c.376-161A>G rs75821853 0.17549
NM_000546.6(TP53):c.993+577A>T rs60699444 0.17098
NM_000546.6(TP53):c.1101-221G>A rs6503048 0.16051
NM_000546.6(TP53):c.782+92T>G rs12951053 0.09904
NM_000546.6(TP53):c.782+72C>T rs12947788 0.09901
NM_000546.6(TP53):c.993+505G>A rs75732100 0.07732
NM_000546.6(TP53):c.376-125T>C rs9895829 0.07381
NM_000546.6(TP53):c.-28-112G>A rs8079544 0.07375
NM_000546.6(TP53):c.97-29C>A rs17883323 0.07310
NM_000546.6(TP53):c.672+220G>T rs8069054 0.05709
NM_000546.6(TP53):c.*826G>A rs17884306 0.05075
NM_000546.6(TP53):c.993+352C>T rs77697176 0.03428
NM_000546.6(TP53):c.*485G>A rs4968187 0.01815
NM_000546.6(TP53):c.993+12T>C rs1800899 0.01614
NM_000546.6(TP53):c.639A>G (p.Arg213=) rs1800372 0.01275
NM_000546.6(TP53):c.1101-49C>T rs17881850 0.00982
NM_000546.6(TP53):c.108G>A (p.Pro36=) rs1800370 0.00974
NM_000546.6(TP53):c.1100+30A>T rs17880847 0.00929
NM_000546.6(TP53):c.*1175A>C rs78378222 0.00849
NM_000546.6(TP53):c.97-6C>T rs35117667 0.00847
NM_000546.6(TP53):c.376-101A>T rs145153611 0.00226
NM_000546.6(TP53):c.139C>T (p.Pro47Ser) rs1800371 0.00123
NM_000546.6(TP53):c.704A>G (p.Asn235Ser) rs144340710 0.00025
NM_000546.6(TP53):c.216C>T (p.Pro72=) rs56275308 0.00022
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.74+14T>C rs184743157 0.00018
NM_000546.6(TP53):c.869G>A (p.Arg290His) rs55819519 0.00014
NM_000546.6(TP53):c.6G>A (p.Glu2=) rs143458271 0.00009
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.102C>G (p.Pro34=) rs11575998 0.00004
NM_000546.6(TP53):c.1149C>T (p.Leu383=) rs373710656 0.00004
NM_000546.6(TP53):c.246G>A (p.Pro82=) rs372397095 0.00004
NM_000546.6(TP53):c.91G>A (p.Val31Ile) rs201753350 0.00004
NM_000546.6(TP53):c.180A>C (p.Pro60=) rs749289195 0.00003
NM_000546.6(TP53):c.459C>T (p.Pro153=) rs72661116 0.00003
NM_000546.6(TP53):c.903A>G (p.Pro301=) rs72661120 0.00003
NM_000546.6(TP53):c.468C>T (p.Arg156=) rs761222871 0.00002
NM_000546.6(TP53):c.123T>C (p.Asp41=) rs369129220 0.00001
NM_000546.6(TP53):c.354A>T (p.Thr118=) rs751978853 0.00001
NM_000546.6(TP53):c.75-18T>G rs1273569924 0.00001
NM_000546.6(TP53):c.783-11A>G rs771914358 0.00001
NC_000017.11:g.7668174_7668179dup rs17880560
NM_000546.6(TP53):c.-28-317del rs34576726
NM_000546.6(TP53):c.-28-318_-28-317del rs34576726
NM_000546.6(TP53):c.147T>C (p.Asp49=) rs786201148
NM_000546.6(TP53):c.336C>A (p.Gly112=) rs876659177
NM_000546.6(TP53):c.376-160_376-158del rs5819162
NM_000546.6(TP53):c.63C>T (p.Asp21=) rs1800369
NM_000546.6(TP53):c.666G>T (p.Pro222=) rs72661118
NM_000546.6(TP53):c.672+48G>A rs17884607
NM_000546.6(TP53):c.673-36G>C rs17880604
NM_000546.6(TP53):c.96+18del rs730882012
NM_000546.6(TP53):c.96+41_97-54del rs59758982
NM_000546.6(TP53):c.993+391_993+392dup rs34308401
NM_000546.6(TP53):c.993+409del rs34308401

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