Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
PTPN12	9645	COSM142819,	skin	malignant_melanoma	p.S483L	Substitution - Missense	7:77627127-77627127,	PATHOGENIC	0.93837	19074898
PTPN12	9645	COSM142820,	skin	malignant_melanoma	p.P772S	Substitution - Missense	7:77639251-77639251,	PATHOGENIC	0.92404	19074898
PTPN12	9645	COSM142818,	skin	malignant_melanoma	p.V313G	Substitution - Missense	7:77611045-77611045,	PATHOGENIC	0.91428	19074898
PTPN12	9645	COSM5019354,	soft_tissue	haemangioblastoma	p.?	Unknown	7:77571075-77571075,	PATHOGENIC	0.79612	25589003
PTPN12	9645	COSM5019354,	soft_tissue	haemangioblastoma	p.?	Unknown	7:77571075-77571075,	PATHOGENIC	0.79612	25589003
PTPN12	9645	COSM5019354,	soft_tissue	haemangioblastoma	p.?	Unknown	7:77571075-77571075,	PATHOGENIC	0.79612	25589003
PTPN12	9645	COSM5019354,	soft_tissue	haemangioblastoma	p.?	Unknown	7:77571075-77571075,	PATHOGENIC	0.79612	25589003
PTPN12	9645	COSM5019354,	soft_tissue	haemangioblastoma	p.?	Unknown	7:77571075-77571075,	PATHOGENIC	0.79612	25589003
PTPN12	9645	COSM5019354,	soft_tissue	haemangioblastoma	p.?	Unknown	7:77571075-77571075,	PATHOGENIC	0.79612	25589003
PTPN12	9645	COSM5019354,	soft_tissue	haemangioblastoma	p.?	Unknown	7:77571075-77571075,	PATHOGENIC	0.79612	25589003
PTPN12	9645	COSM5019354,	soft_tissue	haemangioblastoma	p.?	Unknown	7:77571075-77571075,	PATHOGENIC	0.79612	25589003
PTPN12	9645	COSM5019354,	soft_tissue	haemangioblastoma	p.?	Unknown	7:77571075-77571075,	PATHOGENIC	0.79612	25589003
PTPN12	9645	COSM5019354,	soft_tissue	haemangioblastoma	p.?	Unknown	7:77571075-77571075,	PATHOGENIC	0.79612	25589003
PTPN12	9645	COSM3762840,	soft_tissue	haemangioblastoma	p.T573A	Substitution - Missense	7:77627396-77627396,	NEUTRAL	0.06193	25589003
PTPN12	9645	COSM3762840,	soft_tissue	haemangioblastoma	p.T573A	Substitution - Missense	7:77627396-77627396,	NEUTRAL	0.06193	25589003
PTPN12	9645	COSM3762840,	soft_tissue	haemangioblastoma	p.T573A	Substitution - Missense	7:77627396-77627396,	NEUTRAL	0.06193	25589003
PTPN12	9645	COSM3762840,	soft_tissue	haemangioblastoma	p.T573A	Substitution - Missense	7:77627396-77627396,	NEUTRAL	0.06193	25589003
PTPN12	9645	COSM3762840,	soft_tissue	haemangioblastoma	p.T573A	Substitution - Missense	7:77627396-77627396,	NEUTRAL	0.06193	25589003
PTPN12	9645	COSM3762840,	soft_tissue	haemangioblastoma	p.T573A	Substitution - Missense	7:77627396-77627396,	NEUTRAL	0.06193	25589003
PTPN12	9645	COSM3762840,	soft_tissue	haemangioblastoma	p.T573A	Substitution - Missense	7:77627396-77627396,	NEUTRAL	0.06193	25589003
PTPN12	9645	COSM3762840,	soft_tissue	haemangioblastoma	p.T573A	Substitution - Missense	7:77627396-77627396,	NEUTRAL	0.06193	25589003
PTPN12	9645	COSM3762840,	soft_tissue	haemangioblastoma	p.T573A	Substitution - Missense	7:77627396-77627396,	NEUTRAL	0.06193	25589003
PTPN12	9645	COSM3762840,	soft_tissue	haemangioblastoma	p.T573A	Substitution - Missense	7:77627396-77627396,	NEUTRAL	0.06193	25589003
PTPN12	9645	COSM5019270,	soft_tissue	haemangioblastoma	p.E706K	Substitution - Missense	7:77635823-77635823,	Info_not_available	0.66449	25589003