Gene Name	HGNC ID	COSMIC_MutID	Primary site	Primary histology	AA-Mutation	Mutation Type	Genomic Position	FATHMM prediction	FATHMM score	Literature evidence
NFAT5	7774	COSM5049148,	oesophagus	carcinoma	p.I292V	Substitution - Missense	16:69655759-69655759,	PATHOGENIC	0.99818	24686850
NFAT5	7774	COSM5047326,	oesophagus	carcinoma	p.K25N	Substitution - Missense	16:69647131-69647131,	PATHOGENIC	0.87172	24686850