Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
SKP2	10901	COSM39467,	central_nervous_system	glioma	p.S168L	Substitution - Missense	5:36166629-36166629,	PATHOGENIC	0.96413	18772396
SKP2	10901	COSM39466,	central_nervous_system	glioma	p.S135F	Substitution - Missense	5:36166530-36166530,	PATHOGENIC	0.94376	18772396
SKP2	10901	COSM96209,	breast	carcinoma	p.K71K	Substitution - coding silent	5:36152975-36152975,	Info_not_available	0.52273	20668451