List of variants in gene TP53 reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.460G>A (p.Gly154Ser)	rs137852789	0.00004
NM_000546.6(TP53):c.998G>A (p.Arg333His)	rs573154688	0.00004
NM_000546.6(TP53):c.665C>T (p.Pro222Leu)	rs146340390	0.00002
NM_000546.6(TP53):c.784G>A (p.Gly262Ser)	rs200579969	0.00002
NM_000546.6(TP53):c.1078G>A (p.Gly360Arg)	rs786203298	0.00001
NM_000546.6(TP53):c.1150A>G (p.Met384Val)	rs730882009	0.00001
NM_000546.6(TP53):c.376-2dup	rs751253294	0.00001
NM_000546.6(TP53):c.480G>A (p.Met160Ile)	rs772354334	0.00001
NM_000546.6(TP53):c.848G>A (p.Arg283His)	rs371409680	0.00001
NM_000546.6(TP53):c.1115A>G (p.Lys372Arg)	rs876658876
NM_000546.6(TP53):c.322G>A (p.Gly108Ser)	rs587782461
NM_000546.6(TP53):c.358A>C (p.Lys120Gln)	rs121912658
NM_000546.6(TP53):c.515T>A (p.Val172Asp)	rs1131691021
NM_000546.6(TP53):c.528C>G (p.Cys176Trp)	rs1057519980
NM_000546.6(TP53):c.546C>G (p.Cys182Trp)	rs1064796257
NM_000546.6(TP53):c.787A>G (p.Asn263Asp)	rs72661119
NM_000546.6(TP53):c.830G>T (p.Cys277Phe)	rs763098116
NM_000546.6(TP53):c.950A>G (p.Gln317Arg)	rs1159579789
NM_000546.6(TP53):c.997C>T (p.Arg333Cys)	rs769934890

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.