Table 2.

Cases of IHC and TP53 mutation type mismatching (order by AA sequence).

Type	AA Change	Domain	Mutation Type	IHC Staining	Tumor %	VAF
endometrioid	V73W fs*50	TD	FSD	WT	30	10.3
clear cell	G105R	DBD	MM	WT	80	49.88
HGSCa	S183*	DBD	NM	“All”	70	42.67
HGSCa	F212_H214del	DBD	IFD	“All”	70	13.62
endometrioid	S261_G262dup	DBD	IFI	WT	40	16.71
HGSCa	G262del	DBD	IFD	“All”	80	32.92
HGSCa	R273H	DBD	MM	“None”	90	0.75
HGSCa	L289F fs*57	DBD	FSI	Cyto	70	23.66
HGSCa	P301Q fs*44	NLS	FSD	WT	60	27.28
HGSCa	P301Q fs*44	NLS	FSD	“All”	90	82.71
HGSCa	R306*	NLS	NM	Cyto	80	0.86
HGSCa	R306*	NLS	NM	WT + Cyto	80	0.60
HGSCa	R342E fs*3	OD	FSI	“All”	30	36.69
HGSCa	R342*	OD	NM	“All” + Cyto	90	37.4
HGSCa	R342*	OD	NM	“All”	50	7.08
HGSCa	R342*	OD	NM	“All”	60	44.4
HGSCa	E343*	OD	NM	WT	90	0.31
HGSCa	E346*	OD	NM	“All”	90	0.35