Mutation details:

Protein level identifier (NP_060575):

p.Arg29Pro

cDNA level identifier (NM_018105):

c.86G>C

Gene level identifier:

g.3959G>C

Reference, alternative allele:

C, G

Genomic location hg(19)

8:42694510 (not available on ExAC)

Gene name:

THAP1

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

33

Positive functional evidence:

not available

Number of all included cases:

2 heterozygous (2 in total).

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