Mutation details:

Protein level identifier:

p.Gly192Trpfs*8

cDNA level identifier:

c.573dupT

Genome level identifier:

g.1772dupT

Reference, alternative allele:

A, AT

Genetic location (hg19):

chr16:29824947 (not available on ExAC)

Gene name:

PRRT2

Consequence:

frameshift

Pathogenicity scoring:

probably pathogenic

CADD score:

25

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).

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