Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
TIMM50	23656	COSM1581815,	haematopoietic_and_lymphoid_tissue	lymphoid_neoplasm	p.R448C	Substitution - Missense	19:39489791-39489791,	PATHOGENIC	0.92067	23292937
TIMM50	23656	COSM5762967,	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm	p.G159A	Substitution - Missense	19:39481941-39481941,	NEUTRAL	0.18272	27127180
TIMM50	23656	COSM6498565,	haematopoietic_and_lymphoid_tissue	haematopoietic_neoplasm	p.G65fs*119	Deletion - Frameshift	19:39480737-39480737,	Info_not_available	Info_not_available	27486981