Mutation details:

Protein level identifier (NP_000152):

p.Gln219Thrfs*31

cDNA level identifier (NM_000161):

c.653dupT

Gene level identifier:

g.58736dupT

Reference, alternative allele:

T, TA

Genomic location hg(0)

14:5531083 (not available on ExAC)

Gene name:

GCH1

Consequence:

unknown effect

Pathogenicity scoring:

Probably pathogenic

CADD score:

35

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).