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KCNQ2 gene mutations associated with non-familial benign neonatal seizures (nf-BNS).
| Mutation | Note(s) | References |
|---|---|---|
| c.319C>T/p.L107F | - | (34) |
| c.333_334delGT/p.Ser113HisfsX6 | - | (21) |
| c.683C>T/p.R213W | Associated with c.1241A>G/p.E414G in KCNQ3 gene (inherited from mother; polymorphism in Japanese population) | (35) |
| c.901G>A/p.G301S | - | (23) |
| c.910delTTC or TTT/p.F304del | Evolution to BECTS | (36) |
| c.1065C>G/p.D355Q | - | (23) |
| c.1657C>T/p.R553W | - | (34) |
| c.1657C>T/p.R553W | - | (23) |
| c.1700T>A/p.V567D | - | (21) |
