Mutation details:

Protein level identifier (NP_000152):

p.Ala98Thr

cDNA level identifier (NM_000161):

c.292G>A

Gene level identifier:

g.481G>A

Reference, alternative allele:

C, T

Genomic location hg(0)

14:55369090 (not available on ExAC)

Gene name:

GCH1

Consequence:

missense

Pathogenicity scoring:

Possibly pathogenic

CADD score:

24

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).