ClinVar Miner

List of variants in gene TP53 reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.215C>G (p.Pro72Arg) rs1042522 0.62654
NM_000546.6(TP53):c.*773C>T rs200378797 0.06166
NM_000546.6(TP53):c.*826G>A rs17884306 0.05075
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.*569_*570del rs1555523911 0.01175
NM_000546.6(TP53):c.108G>A (p.Pro36=) rs1800370 0.00974
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.*205G>A rs16956880 0.00497
NM_000546.6(TP53):c.*328G>A rs17881366 0.00463
NM_001126113.2(TP53):c.*1422G>C rs17883782 0.00377
NM_000546.6(TP53):c.*613C>A rs17879353 0.00271
NM_000546.6(TP53):c.*409C>A rs191918079 0.00224
NM_000546.6(TP53):c.*357T>C rs534624315 0.00197
NM_000546.6(TP53):c.139C>T (p.Pro47Ser) rs1800371 0.00123
NM_000546.6(TP53):c.*936A>G rs55817367 0.00042
NM_000546.6(TP53):c.*1132C>T rs1044102603 0.00035
NM_000546.6(TP53):c.1014C>T (p.Phe338=) rs150293825 0.00018
NM_000546.6(TP53):c.935C>G (p.Thr312Ser) rs145151284 0.00018
NM_000546.6(TP53):c.*760T>C rs935743951 0.00011
NM_000546.6(TP53):c.1015G>A (p.Glu339Lys) rs17882252 0.00006
NM_000546.6(TP53):c.782+12C>T rs17881780 0.00005
NM_000546.6(TP53):c.91G>A (p.Val31Ile) rs201753350 0.00004
NM_000546.6(TP53):c.*327C>T rs886053512 0.00002
NM_000546.6(TP53):c.-22G>A rs1348969852 0.00001
NM_000546.6(TP53):c.145G>A (p.Asp49Asn) rs587780728 0.00001
NM_000546.6(TP53):c.74+9A>C rs1057517593 0.00001
NM_000546.6(TP53):c.844C>T (p.Arg282Trp) rs28934574 0.00001
NM_000546.6(TP53):c.96+15T>C rs200053580 0.00001
NM_000546.6(TP53):c.*1070C>T rs114831472
NM_000546.6(TP53):c.*1160T>G rs886053499
NM_000546.6(TP53):c.*144G>A rs371002418
NM_000546.6(TP53):c.*168C>T rs2072818956
NM_000546.6(TP53):c.*346G>T rs886053511
NM_000546.6(TP53):c.*347T>C rs886053510
NM_000546.6(TP53):c.*382C>T rs886053509
NM_000546.6(TP53):c.*548G>T rs886053508
NM_000546.6(TP53):c.*565G>T rs886053507
NM_000546.6(TP53):c.*626C>T rs886053506
NM_000546.6(TP53):c.*735C>A rs886053505
NM_000546.6(TP53):c.*747C>T rs886053504
NM_000546.6(TP53):c.*754C>T rs199729221
NM_000546.6(TP53):c.*761T>C rs925506797
NM_000546.6(TP53):c.*772del rs200757381
NM_000546.6(TP53):c.*779del rs886053503
NM_000546.6(TP53):c.*790G>A rs886053502
NM_000546.6(TP53):c.*806C>A rs886053501
NM_000546.6(TP53):c.*977G>C rs886053500
NM_000546.6(TP53):c.*99G>A rs886053513
NM_000546.6(TP53):c.1093C>T (p.His365Tyr) rs267605075
NM_000546.6(TP53):c.145G>C (p.Asp49His) rs587780728
NM_000546.6(TP53):c.18A>G (p.Ser6=) rs573130482
NM_000546.6(TP53):c.318dup (p.Tyr107fs)
NM_000546.6(TP53):c.31G>C (p.Glu11Gln) rs201382018
NM_000546.6(TP53):c.63C>T (p.Asp21=) rs1800369
NM_000546.6(TP53):c.993+8G>A rs1060504163

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