Mutation details:

Protein level identifier (NP_000208):

p.Cys185Trp

cDNA level identifier (NM_000217):

c.555C>G

Gene level identifier:

g.2029C>G

Reference, alternative allele:

C, G

Genomic location hg(19)

12:5021099 (not available on ExAC)

Gene name:

KCNA1

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

25

Positive functional evidence:

not available

Number of all included cases:

3 heterozygous (3 in total).