ClinVar Miner

List of variants in gene TP53 reported as benign for Hereditary cancer-predisposing syndrome

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Gene type:
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Total variants: 47
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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
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.97-29C>A rs17883323 0.07310
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.108G>A (p.Pro36=) rs1800370 0.00974
NM_000546.6(TP53):c.1100+30A>T rs17880847 0.00929
NM_000546.6(TP53):c.97-6C>T rs35117667 0.00847
NM_000546.5(TP53):c.*1701G>T rs183153328 0.00661
NM_000546.6(TP53):c.782+17C>T rs17880172 0.00184
NM_000546.6(TP53):c.139C>T (p.Pro47Ser) rs1800371 0.00123
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.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.935C>G (p.Thr312Ser) rs145151284 0.00018
NM_000546.6(TP53):c.869G>A (p.Arg290His) rs55819519 0.00014
NM_000546.6(TP53):c.97-9C>T rs202217267 0.00011
NM_000546.6(TP53):c.474C>T (p.Arg158=) rs139200646 0.00009
NM_000546.6(TP53):c.248C>T (p.Ala83Val) rs201717599 0.00006
NM_000546.6(TP53):c.903A>G (p.Pro301=) rs72661120 0.00003
NM_000546.6(TP53):c.96+15_96+26del rs765932887 0.00002
NC_000017.11:g.7668174_7668179dup rs17880560
NM_000546.6(TP53):c.386C>A (p.Ala129Asp)
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.673-19G>A rs564974117
NM_000546.6(TP53):c.673-36G>C rs17880604
NM_000546.6(TP53):c.673-44C>T
NM_000546.6(TP53):c.74+38C>A rs1642785
NM_000546.6(TP53):c.932A>G (p.Asn311Ser) rs56184981
NM_000546.6(TP53):c.96+15_96+30del rs730882010
NM_000546.6(TP53):c.96+15_96+31del rs730882011
NM_000546.6(TP53):c.96+41_97-54del rs59758982
NM_000546.6(TP53):c.993+223T>G rs3021068
NM_000546.6(TP53):c.993+326_993+341del rs730882013

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