List of variants in gene TP53 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.28G>A (p.Val10Ile)	rs535274413	0.00004
NM_000546.6(TP53):c.460G>A (p.Gly154Ser)	rs137852789	0.00004
NM_000546.6(TP53):c.105G>C (p.Leu35Phe)	rs121912661	0.00003
NM_000546.6(TP53):c.329G>A (p.Arg110His)	rs11540654	0.00003
NM_000546.6(TP53):c.665C>T (p.Pro222Leu)	rs146340390	0.00002
NM_000546.6(TP53):c.1003C>T (p.Arg335Cys)	rs375444154	0.00001
NM_000546.6(TP53):c.848G>A (p.Arg283His)	rs371409680	0.00001
NM_000546.6(TP53):c.336CTT[1] (p.Phe113del)	rs764486868
NM_000546.6(TP53):c.478A>G (p.Met160Val)	rs377274728
NM_000546.6(TP53):c.59C>T (p.Ser20Leu)	rs1597376439
NM_000546.6(TP53):c.773A>C (p.Glu258Ala)	rs1060501201

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.