Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
CTTN	3338	COSM3703668,	liver	carcinoma	p.Q134K	Substitution - Missense	11:70414650-70414650,	PATHOGENIC	0.94169	Info_not_available
CTTN	3338	COSM1605162,	liver	carcinoma	p.V238L	Substitution - Missense	11:70420432-70420432,	PATHOGENIC	0.88191	Info_not_available
CTTN	3338	COSM3703665,	liver	carcinoma	p.D133E	Substitution - Missense	11:70414649-70414649,	Info_not_available	0.62004	Info_not_available