Mutation details:

cDNA level identifier (n.a.):

c.1071-1_1112delGCCAGCATGGGCACGTGCCCCAGCAGCTCGTGGCAGCAGTCCC

Gene level identifier:

g.5328_5370delGCCAGCATGGGCACGTGCCCCAGCAGCTCGTGGCAGCAGTCCC

Reference, alternative allele:

GGCCAGCATGGGCACGTGCCCCAGCAGCTCGTGGCAGCAGTCCC, G

Genomic location hg(0)

11:2187737 (not available on ExAC)

Gene name:

TH

Consequence:

splice site

Pathogenicity scoring:

Probably pathogenic

CADD score:

not available

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 compound heterozygous (1 in total).

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