Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
NOS1	7872	COSM2157530,	central_nervous_system	glioma	p.G676C	Substitution - Missense	12:117265426-117265426,	PATHOGENIC	0.99472	23917401
NOS1	7872	COSM2157531,	central_nervous_system	glioma	p.T455I	Substitution - Missense	12:117285259-117285259,	PATHOGENIC	0.98883	23917401
NOS1	7872	COSM2157587,	central_nervous_system	glioma	p.T398I	Substitution - Missense	12:117286201-117286201,	PATHOGENIC	0.9821	23917401
NOS1	7872	COSM935628,	central_nervous_system	glioma	p.V572M	Substitution - Missense	12:117272510-117272510,	PATHOGENIC	0.97757	23917401
NOS1	7872	COSM2157588,	central_nervous_system	glioma	p.R672H	Substitution - Missense	12:117265437-117265437,	PATHOGENIC	0.9753	23917401
NOS1	7872	COSM313285,	lung	carcinoma	p.L1404L	Substitution - coding silent	12:117218125-117218125,	PATHOGENIC	0.95789	22941188
NOS1	7872	COSM313286,	lung	carcinoma	p.N296S	Substitution - Missense	12:117290392-117290392,	PATHOGENIC	0.90694	22941188
NOS1	7872	COSM313288,	lung	carcinoma	p.Q633H	Substitution - Missense	12:117268085-117268085,	PATHOGENIC	0.83645	22941188