Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
PHLPP1	20610	COSM4606095,	upper_aerodigestive_tract	carcinoma	p.?	Unknown	18:62902963-62902963,	PATHOGENIC	0.9975	25056374
PHLPP1	20610	COSM4072906,	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm	p.P1499L	Substitution - Missense	18:62978773-62978773,	PATHOGENIC	0.93361	27486981
PHLPP1	20610	COSM4604947,	upper_aerodigestive_tract	carcinoma	p.E1426K	Substitution - Missense	18:62978553-62978553,	PATHOGENIC	0.9284	25056374
PHLPP1	20610	COSM4606081,	upper_aerodigestive_tract	carcinoma	p.S515W	Substitution - Missense	18:62717227-62717227,	PATHOGENIC	0.71293	25056374
PHLPP1	20610	COSM4606321,	upper_aerodigestive_tract	carcinoma	p.S164L	Substitution - Missense	18:62716174-62716174,	NEUTRAL	0.42037	25056374
PHLPP1	20610	COSM1611343,	liver	carcinoma	p.?	Unknown	18:62920118-62920118,	NEUTRAL	0.16289	Info_not_available
PHLPP1	20610	COSM5762917,	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm	p.S323P	Substitution - Missense	18:62716650-62716650,	NEUTRAL	0.04321	27127180