ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 57
Download table as spreadsheet
HGVS dbSNP
NM_000546.6(TP53):c.*1132C>T
NM_000546.6(TP53):c.*144G>A
NM_000546.6(TP53):c.*168C>T
NM_000546.6(TP53):c.*328G>A
NM_000546.6(TP53):c.*357T>C
NM_000546.6(TP53):c.*409C>A
NM_000546.6(TP53):c.*760T>C
NM_000546.6(TP53):c.*761T>C
NM_000546.6(TP53):c.-22G>A
NM_000546.6(TP53):c.1093C>T (p.His365Tyr) rs267605075
NM_000546.6(TP53):c.139C>T (p.Pro47Ser) rs1800371
NM_000546.6(TP53):c.215C>G (p.Pro72Arg) rs1042522
NM_000546.6(TP53):c.31G>C (p.Glu11Gln) rs201382018
NM_000546.6(TP53):c.639A>G (p.Arg213=) rs1800372
NM_000546.6(TP53):c.844C>T (p.Arg282Trp) rs28934574
NM_000546.6(TP53):c.91G>A (p.Val31Ile) rs201753350
NM_000546.6(TP53):c.935C>G (p.Thr312Ser) rs145151284
NM_001126112.2(TP53):c.*1070C>T rs114831472
NM_001126112.2(TP53):c.*1160T>G rs886053499
NM_001126112.2(TP53):c.*1175A>C rs78378222
NM_001126112.2(TP53):c.*205G>A rs16956880
NM_001126112.2(TP53):c.*327C>T rs886053512
NM_001126112.2(TP53):c.*346G>T rs886053511
NM_001126112.2(TP53):c.*347T>C rs886053510
NM_001126112.2(TP53):c.*382C>T rs886053509
NM_001126112.2(TP53):c.*485G>A rs4968187
NM_001126112.2(TP53):c.*548G>T rs886053508
NM_001126112.2(TP53):c.*565G>T rs886053507
NM_001126112.2(TP53):c.*569_*570del rs1555523911
NM_001126112.2(TP53):c.*613C>A rs17879353
NM_001126112.2(TP53):c.*626C>T rs886053506
NM_001126112.2(TP53):c.*735C>A rs886053505
NM_001126112.2(TP53):c.*747C>T rs886053504
NM_001126112.2(TP53):c.*754C>T rs199729221
NM_001126112.2(TP53):c.*772del rs200757381
NM_001126112.2(TP53):c.*773C>T rs200378797
NM_001126112.2(TP53):c.*779del rs886053503
NM_001126112.2(TP53):c.*790G>A rs886053502
NM_001126112.2(TP53):c.*806C>A rs886053501
NM_001126112.2(TP53):c.*826G>A rs17884306
NM_001126112.2(TP53):c.*936A>G rs55817367
NM_001126112.2(TP53):c.*977G>C rs886053500
NM_001126112.2(TP53):c.*99G>A rs886053513
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.108G>A (p.Pro36=) rs1800370
NM_001126112.2(TP53):c.145G>A (p.Asp49Asn) rs587780728
NM_001126112.2(TP53):c.145G>C (p.Asp49His) rs587780728
NM_001126112.2(TP53):c.18A>G (p.Ser6=) rs573130482
NM_001126112.2(TP53):c.63C>T (p.Asp21=) rs1800369
NM_001126112.2(TP53):c.74+9A>C rs1057517593
NM_001126112.2(TP53):c.782+12C>T rs17881780
NM_001126112.2(TP53):c.96+15T>C rs200053580
NM_001126112.2(TP53):c.97-6C>T rs35117667
NM_001126112.2(TP53):c.993+12T>C rs1800899
NM_001126112.2(TP53):c.993+8G>A rs1060504163
NM_001126113.2(TP53):c.*1422G>C rs17883782

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.