Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
PRKCA	9393	COSM4604235,	upper_aerodigestive_tract	carcinoma	p.Q430R	Substitution - Missense	17:66738822-66738822,	PATHOGENIC	0.99803	25056374
PRKCA	9393	COSM95071,	lung	carcinoma	p.D641G	Substitution - Missense	17:66803940-66803940,	PATHOGENIC	0.98695	20668451
PRKCA	9393	COSM4604407,	upper_aerodigestive_tract	carcinoma	p.G525D	Substitution - Missense	17:66774036-66774036,	PATHOGENIC	0.98284	25056374
PRKCA	9393	COSM20476,	large_intestine	carcinoma	p.P98S	Substitution - Missense	17:66641358-66641358,	PATHOGENIC	0.97642	Info_not_available
PRKCA	9393	COSM20476,	large_intestine	carcinoma	p.P98S	Substitution - Missense	17:66641358-66641358,	PATHOGENIC	0.97642	Info_not_available
PRKCA	9393	COSM20989,	central_nervous_system	glioma	p.D467N	Substitution - Missense	17:66742635-66742635,	PATHOGENIC	0.9647	Info_not_available
PRKCA	9393	COSM20989,	central_nervous_system	glioma	p.D467N	Substitution - Missense	17:66742635-66742635,	PATHOGENIC	0.9647	16618716
PRKCA	9393	COSM20989,	central_nervous_system	glioma	p.D467N	Substitution - Missense	17:66742635-66742635,	PATHOGENIC	0.9647	Info_not_available
PRKCA	9393	COSM20989,	central_nervous_system	glioma	p.D467N	Substitution - Missense	17:66742635-66742635,	PATHOGENIC	0.9647	16618716
PRKCA	9393	COSM95070,	breast	carcinoma	p.S272N	Substitution - Missense	17:66688430-66688430,	PATHOGENIC	0.88463	20668451
PRKCA	9393	COSM4603851,	upper_aerodigestive_tract	carcinoma	p.E282delE	Deletion - In frame	17:66688968-66688970,	Info_not_available	Info_not_available	25056374
PRKCA	9393	COSM20523,	stomach	carcinoma	p.N182fs*2	Deletion - Frameshift	17:66687121-66687121,	Info_not_available	Info_not_available	Info_not_available