Mutation details:

Protein level identifier (NP_000152):

p.Gly21Glufs*47

cDNA level identifier (NM_000161):

c.61_62delGGinsAACC

Gene level identifier:

g.250_251delGGinsAACC

Reference, alternative allele:

ACC, AGGTT

Genomic location hg(0)

14:55369320 (not available on ExAC)

Gene name:

GCH1

Consequence:

unknown effect

Pathogenicity scoring:

Definitely pathogenic

CADD score:

24

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).