The epilepsy gene panel search strategy identified de novo variants in two well‐known epilepsy genes: c.2359C>T (p.R787C), a novel variant in the GABABR2 subunit gene (GABBR2), and c.748G>A (p.V250I), a previously reported variant in SCN1A.25, 26. The gene discussed is SCN1A; the disease is epilepsy.