FGFR2 and infantile convulsions and choreoathetosis: Overall, the most commonly mutated genes among all iCCA patients were TP53 (21%), IDH1 (20%), BAP1 (17%), ARID1A (16%), FGFR2 (16%), CDKN2A (14%), CDKN2B (12%), KRAS (12%), and PBRM1 (12%).