List of variants in gene TP53 reported by Cancer Variant Interpretation Group UK, Institute of Cancer Research, London

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.998G>A (p.Arg333His)	rs573154688	0.00004
NM_000546.6(TP53):c.1010G>A (p.Arg337His)	rs121912664	0.00001
NM_000546.6(TP53):c.374C>T (p.Thr125Met)	rs786201057	0.00001
NM_000546.6(TP53):c.472C>T (p.Arg158Cys)	rs587780068	0.00001
NM_000546.6(TP53):c.542G>A (p.Arg181His)	rs397514495	0.00001
NM_000546.6(TP53):c.1141A>G (p.Lys381Glu)	rs2072835371
NM_000546.6(TP53):c.322G>C (p.Gly108Arg)	rs587782461
NM_000546.6(TP53):c.453_455del (p.Pro153del)	rs730882019
NM_000546.6(TP53):c.560-14_560-13del	rs2073351616
NM_000546.6(TP53):c.623A>G (p.Asp208Gly)	rs1464727668
NM_000546.6(TP53):c.646G>A (p.Val216Met)	rs730882025
NM_000546.6(TP53):c.794T>A (p.Leu265Gln)	rs879253942
NM_000546.6(TP53):c.799C>T (p.Arg267Trp)	rs55832599

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.