Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
PTPRN2	9677	COSM142755,	skin	malignant_melanoma	p.E717K	Substitution - Missense	7:157656404-157656404,	PATHOGENIC	0.94434	19074898
PTPRN2	9677	COSM32659,	large_intestine	carcinoma	p.E716K	Substitution - Missense	7:157656407-157656407,	PATHOGENIC	0.94434	16959974
PTPRN2	9677	COSM142754,	skin	malignant_melanoma	p.D68N	Substitution - Missense	7:158316894-158316894,	PATHOGENIC	0.94219	19074898
PTPRN2	9677	COSM142758,	skin	malignant_melanoma	p.P257L	Substitution - Missense	7:158167071-158167071,	NEUTRAL	0.05798	19074898
PTPRN2	9677	COSM1622645,	liver	carcinoma	p.E493K	Substitution - Missense	7:158133756-158133756,	NEUTRAL	0.03167	Info_not_available
PTPRN2	9677	COSM314599,	lung	carcinoma	p.R387I	Substitution - Missense	7:158136668-158136668,	NEUTRAL	0.03133	22941188
PTPRN2	9677	COSM109159,	skin	malignant_melanoma	p.A355T	Substitution - Missense	7:158138363-158138363,	NEUTRAL	0.00837	19074898
PTPRN2	9677	COSM5026867,	breast	carcinoma	p.A182T	Substitution - Missense	7:158192332-158192332,	NEUTRAL	0.00658	22722193
PTPRN2	9677	COSM142756,	skin	malignant_melanoma	p.R179K	Substitution - Missense	7:158192340-158192340,	NEUTRAL	0.00434	19074898
PTPRN2	9677	COSM142757,	skin	malignant_melanoma	p.G143D	Substitution - Missense	7:158192448-158192448,	NEUTRAL	0.00273	19074898
PTPRN2	9677	COSM142759,	skin	malignant_melanoma	p.M423I	Substitution - Missense	7:158133964-158133964,	NEUTRAL	0.00185	19074898
PTPRN2	9677	COSM142760,	skin	malignant_melanoma	p.P759L	Substitution - Missense	7:157621430-157621430,	Info_not_available	0.62434	19074898