Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
LPIN2	14450	COSM5049248,	oesophagus	carcinoma	p.P539L	Substitution - Missense	18:2928595-2928595,	PATHOGENIC	0.99462	24686850
LPIN2	14450	COSM5028409,	breast	carcinoma	p.?	Unknown	18:2940713-2940713,	PATHOGENIC	0.99378	22722193
LPIN2	14450	COSM3717884,	liver	carcinoma	p.S60F	Substitution - Missense	18:2960662-2960662,	PATHOGENIC	0.9544	Info_not_available
LPIN2	14450	COSM312573,	lung	carcinoma	p.S472S	Substitution - coding silent	18:2931296-2931296,	NEUTRAL	0.08657	22941188