ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
Download table as spreadsheet
HGVS dbSNP
NM_000546.5(TP53):c.*1701G>T rs183153328
NM_000546.5(TP53):c.1079G>C (p.Gly360Ala) rs35993958
NM_000546.5(TP53):c.108G>A (p.Pro36=) rs1800370
NM_000546.5(TP53):c.139C>T (p.Pro47Ser) rs1800371
NM_000546.5(TP53):c.145G>A (p.Asp49Asn) rs587780728
NM_000546.5(TP53):c.215C>G (p.Pro72Arg) rs1042522
NM_000546.5(TP53):c.217G>A (p.Val73Met) rs587782423
NM_000546.5(TP53):c.245C>T (p.Pro82Leu) rs534447939
NM_000546.5(TP53):c.248C>T (p.Ala83Val) rs201717599
NM_000546.5(TP53):c.256G>A (p.Ala86Thr) rs587782148
NM_000546.5(TP53):c.639A>G (p.Arg213=) rs1800372
NM_000546.5(TP53):c.666G>T (p.Pro222=) rs72661118
NM_000546.5(TP53):c.704A>G (p.Asn235Ser) rs144340710
NM_000546.5(TP53):c.74+38C>A rs1642785
NM_000546.5(TP53):c.74+38C>G rs1642785
NM_000546.5(TP53):c.869G>A (p.Arg290His) rs55819519
NM_000546.5(TP53):c.935C>G (p.Thr312Ser) rs145151284
NM_000546.5(TP53):c.96+15_96+26del
NM_000546.5(TP53):c.96+15_96+30del16 rs730882010
NM_000546.5(TP53):c.96+15_96+31del rs730882011
NM_000546.5(TP53):c.96+16_96+31del16 rs59758982
NM_000546.5(TP53):c.96+16delG rs730882012
NM_000546.5(TP53):c.97-6C>T rs35117667
NM_000546.5(TP53):c.993+12T>C rs1800899
NM_000546.5(TP53):c.993+223T>G rs3021068
NM_000546.5(TP53):c.993+326_993+341del16 rs730882013

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.