Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
CDK2	1771	COSM13309,	central_nervous_system	glioma	p.P45L	Substitution - Missense	12:55967874-55967874,	PATHOGENIC	0.94867	16618716
CDK2	1771	COSM13309,	central_nervous_system	glioma	p.P45L	Substitution - Missense	12:55967874-55967874,	PATHOGENIC	0.94867	16618716
CDK2	1771	COSM98878,	stomach	carcinoma	p.R245Q	Substitution - Missense	12:55971189-55971189,	PATHOGENIC	0.78825	21097718
CDK2	1771	COSM5019698,	soft_tissue	haemangioblastoma	p.E28E	Substitution - coding silent	12:55967092-55967092,	NEUTRAL	0.45136	25589003
CDK2	1771	COSM5019698,	soft_tissue	haemangioblastoma	p.E28E	Substitution - coding silent	12:55967092-55967092,	NEUTRAL	0.45136	25589003
CDK2	1771	COSM5019698,	soft_tissue	haemangioblastoma	p.E28E	Substitution - coding silent	12:55967092-55967092,	NEUTRAL	0.45136	25589003
CDK2	1771	COSM5019698,	soft_tissue	haemangioblastoma	p.E28E	Substitution - coding silent	12:55967092-55967092,	NEUTRAL	0.45136	25589003
CDK2	1771	COSM5017284,	kidney	carcinoma	p.E12fs*14	Deletion - Frameshift	12:55967043-55967043,	Info_not_available	Info_not_available	25401301