Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
LMNB1	31682/6637	COSM1619373,	liver	carcinoma	p.K528K	Substitution - coding silent	5:126826080-126826080,	PATHOGENIC	0.8878	Info_not_available
LMNB1	31682/6637	COSM40261,	central_nervous_system	glioma	p.E69K	Substitution - Missense	5:126777713-126777713,	PATHOGENIC	0.87137	18772396
LMNB1	31682/6637	COSM1166751,	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm	p.L184fs*8	Deletion - Frameshift	5:126805602-126805605,	Info_not_available	Info_not_available	22976956