Mutation details:

Protein level identifier (NP_060575):

p.Gln167*

cDNA level identifier (NM_018105):

c.499C>T

Gene level identifier:

g.5221C>T

Reference, alternative allele:

G, A

Genomic location hg(19)

8:42693248 (not available on ExAC)

Gene name:

THAP1

Consequence:

nonsense

Pathogenicity scoring:

Probably pathogenic

CADD score:

38

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).