Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
PTPRZ1	9685	COSM5047775,	oesophagus	carcinoma	p.?	Unknown	7:122058798-122058798,	PATHOGENIC	0.9921	24686850
PTPRZ1	9685	COSM2766487,	oesophagus	carcinoma	p.W49*	Substitution - Nonsense	7:121967972-121967972,	PATHOGENIC	0.98816	24686850
PTPRZ1	9685	COSM2766489,	oesophagus	carcinoma	p.W49*	Substitution - Nonsense	7:121967973-121967973,	PATHOGENIC	0.98816	24686850
PTPRZ1	9685	COSM5047578,	oesophagus	carcinoma	p.G1415D	Substitution - Missense	7:122013290-122013290,	PATHOGENIC	0.92875	24686850
PTPRZ1	9685	COSM50772,	large_intestine	carcinoma	p.C2144F	Substitution - Missense	7:122054990-122054990,	PATHOGENIC	0.86996	17932254
PTPRZ1	9685	COSM249540,	kidney	carcinoma	p.M1235V	Substitution - Missense	7:122012749-122012749,	NEUTRAL	0.06546	22138691
PTPRZ1	9685	COSM51036,	large_intestine	carcinoma	p.S2248S	Substitution - coding silent	7:122059825-122059825,	NEUTRAL	0.03965	17932254
PTPRZ1	9685	COSM5026816,	breast	carcinoma	p.T472T	Substitution - coding silent	7:122010462-122010462,	NEUTRAL	0.02209	22722193
PTPRZ1	9685	COSM28036,	kidney	carcinoma	p.A160P	Substitution - Missense	Info_not_available	Info_not_available	Info_not_available	20054297