Mutation details:

Protein level identifier (NP_001035):

p.Pro529Leu

cDNA level identifier (NM_001044):

c.1586C>T

Gene level identifier:

g.39230C>T

Reference, alternative allele:

G, A

Genomic location hg(19)

5:1406316 (not available on ExAC)

Gene name:

SLC6A3

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

not available

Positive functional evidence:

not available

Number of all included cases:

1 compound heterozygous (1 in total).

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