Mutation details:

Protein level identifier (NP_001243371):

p.Arg266Gln

cDNA level identifier (NM_001256442):

c.797G>A

Gene level identifier:

g.1996G>A

Reference, alternative allele:

G, A

Genomic location hg(19)

16:29825172

Gene name:

PRRT2

Consequence:

missense

Pathogenicity scoring:

Possibly pathogenic

CADD score:

21

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).