Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
PTPN14	9647	COSM5025510,	breast	carcinoma	p.S158F	Substitution - Missense	1:214411721-214411721,	PATHOGENIC	0.98905	22722193
PTPN14	9647	COSM314579,	lung	carcinoma	p.A763V	Substitution - Missense	1:214383567-214383567,	PATHOGENIC	0.98769	22941188
PTPN14	9647	COSM32483,	breast	carcinoma	p.Q159E	Substitution - Missense	1:214411719-214411719,	PATHOGENIC	0.98472	16959974
PTPN14	9647	COSM1581553,	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm	p.P1115L	Substitution - Missense	1:214364603-214364603,	PATHOGENIC	0.98025	23292937
PTPN14	9647	COSM1581553,	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm	p.P1115L	Substitution - Missense	1:214364603-214364603,	PATHOGENIC	0.98025	23292937
PTPN14	9647	COSM1581553,	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm	p.P1115L	Substitution - Missense	1:214364603-214364603,	PATHOGENIC	0.98025	23292937
PTPN14	9647	COSM32454,	breast	carcinoma	p.H360P	Substitution - Missense	1:214384776-214384776,	PATHOGENIC	0.89548	16959974
PTPN14	9647	COSM1581554,	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm	p.V759M	Substitution - Missense	1:214383580-214383580,	NEUTRAL	0.26631	23292937
PTPN14	9647	COSM1658952,	salivary_gland	carcinoma	p.P797L	Substitution - Missense	1:214383465-214383465,	NEUTRAL	0.19556	23778141