Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
KSR2		COSM4760527,	kidney	carcinoma	p.T560M	Substitution - Missense	12:117539823-117539823,	PATHOGENIC	0.98865	25401301
KSR2		COSM94589,	lung	carcinoma	p.K965Q	Substitution - Missense	12:117469711-117469711,	PATHOGENIC	0.98643	20668451
KSR2		COSM21259,	lung	carcinoma	p.R429L	Substitution - Missense	12:117582341-117582341,	PATHOGENIC	0.97072	16140923
KSR2		COSM21259,	lung	carcinoma	p.R429L	Substitution - Missense	12:117582341-117582341,	PATHOGENIC	0.97072	Info_not_available
KSR2		COSM21259,	lung	carcinoma	p.R429L	Substitution - Missense	12:117582341-117582341,	PATHOGENIC	0.97072	16140923
KSR2		COSM21259,	lung	carcinoma	p.R429L	Substitution - Missense	12:117582341-117582341,	PATHOGENIC	0.97072	Info_not_available
KSR2		COSM94590,	lung	carcinoma	p.S379R	Substitution - Missense	12:117667604-117667604,	PATHOGENIC	0.96933	20668451
KSR2		COSM50327,	large_intestine	carcinoma	p.T778M	Substitution - Missense	12:117485674-117485674,	PATHOGENIC	0.96777	17932254
KSR2		COSM98914,	stomach	carcinoma	p.R741Q	Substitution - Missense	12:117524945-117524945,	PATHOGENIC	0.96315	21097718
KSR2		COSM48990,	lung	carcinoma	p.?	Unknown	12:117761525-117761525,	PATHOGENIC	0.94624	18948947
KSR2		COSM95981,	breast	carcinoma	p.L963L	Substitution - coding silent	12:117469715-117469715,	PATHOGENIC	0.93642	20668451
KSR2		COSM95982,	lung	carcinoma	p.L369L	Substitution - coding silent	12:117667634-117667634,	PATHOGENIC	0.91906	20668451
KSR2		COSM48911,	lung	carcinoma	p.Q201L	Substitution - Missense	12:117761491-117761491,	PATHOGENIC	0.8255	18948947
KSR2		COSM12863,	lung	carcinoma	p.G719G	Substitution - coding silent	12:117525010-117525010,	NEUTRAL	0.06597	16140923
KSR2		COSM12863,	lung	carcinoma	p.G719G	Substitution - coding silent	12:117525010-117525010,	NEUTRAL	0.06597	16140923