Mutation details:

cDNA level identifier (NM_001044):

c.1156+5delG

Gene level identifier:

g.30745delG

Reference, alternative allele:

TC, T

Genomic location hg(19)

5:1414685 (not available on ExAC)

Gene name:

SLC6A3

Consequence:

splice site

Pathogenicity scoring:

Possibly pathogenic

CADD score:

not available

Positive functional evidence:

not available

Number of all included cases:

1 homozygous (1 in total).

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