Table 3 Potassium channel mutations

ATP12A

NM_001676

Br13X

g.chr13:24178566C>G

c.2134C>G

p.Q712E

Missense

GRIK4

CCDS8433.1

Br17X

g.chr11:120343207G>A

c.2360G>A

p.G787E

Missense

KCNA4

NM_002233

Br29P

g.chr11:29990620C>T

c.182C>T

p.S61F

Missense

KCNB2

CCDS6209.1

Br11P

g.chr8:74011087G>A

c.943G>A

p.A315T

Missense

KCND2

CCDS5776.1

Br03X

g.chr7:119979914C>T

c.1597C>T

p.R533X

Missense

KCNG3

CCDS1809.1

Br26X

g.chr2:42631881G>A

c.412G>A

p.D138N

Missense

KCNH1

CCDS1496.1

Br9PT

g.chr1:207365704G>T

c.1662G>T

p.K554N

Missense

KCNH5

CCDS9756.1

Br08X

g.chr14:62316201C>T

c.2017C>T

p.R673W

Missense

KCNJ15

CCDS13656.1

Br03X

g.chr21:38593138G>A

c.85G>A

p.V29I

Missense

KCNK1

CCDS1599.1

Br26X

g.chr1:230109198G>A

c.478G>A

p.V160I

Missense

LRRC4B

ENST00000253728

Br03X

g.chr19:55713328C>T

c.809C>T

p.T270I

Missense

REN

NM_000537

Br20P

g.chr1:200862821G>A

c.226G>A

p.V76M

Missense

SLC12A5

CCDS13391.1

Br14X

g.chr20:44097883G>A

c.340G>A

p.V114I

Missense