Mutation details:

Protein level identifier (NP_000152):

p.Arg178del

cDNA level identifier (NM_000161):

c.532_534delAGA

Gene level identifier:

g.55745_55747delAGA

Reference, alternative allele:

GTCT, G

Genomic location hg(0)

14:55313823 (not available on ExAC)

Gene name:

GCH1

Consequence:

unknown effect

Pathogenicity scoring:

Probably pathogenic

CADD score:

23

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).