ClinVar Miner

List of variants in gene TP53 reported by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
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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 0.83732
NM_000546.6(TP53):c.672+62A>G rs1625895 0.83418
NM_000546.6(TP53):c.74+38C>G rs1642785 0.65950
NM_000546.6(TP53):c.215C>G (p.Pro72Arg) rs1042522 0.62654
NM_000546.6(TP53):c.376-161A>G rs75821853 0.17549
NM_000546.6(TP53):c.782+72C>T rs12947788 0.10458
NM_000546.6(TP53):c.782+92T>G rs12951053 0.09904
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.376-125T>C rs9895829 0.07302
NM_000546.6(TP53):c.672+220G>T rs8069054 0.05299
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.376-117G>A rs35850753 0.01308
NM_000546.6(TP53):c.639A>G (p.Arg213=) rs1800372 0.01238
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.376-86T>C rs113530090 0.00891
NM_000546.6(TP53):c.97-6C>T rs35117667 0.00785
NM_000546.6(TP53):c.672+31A>G rs34949160 0.00543
NM_000546.6(TP53):c.*205G>A rs16956880 0.00497
NM_000546.6(TP53):c.673-100C>T rs183276131 0.00414
NM_000546.6(TP53):c.*409C>A rs191918079 0.00238
NM_000546.6(TP53):c.376-101A>T rs145153611 0.00226
NM_000546.6(TP53):c.*357T>C rs534624315 0.00192
NM_000546.6(TP53):c.139C>T (p.Pro47Ser) rs1800371 0.00123
NM_000546.6(TP53):c.672+18G>C rs199578278 0.00014
NM_000546.6(TP53):c.28G>A (p.Val10Ile) rs535274413 0.00004
NM_000546.6(TP53):c.*772del rs200757381
NM_000546.6(TP53):c.375+17G>A rs765179201
NM_000546.6(TP53):c.672+48G>T rs17884607
NM_000546.6(TP53):c.673-36G>C rs17880604
NM_000546.6(TP53):c.894G>A (p.Glu298=) rs756123992

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