Mutation details:

Protein level identifier (n.a.):

p.Thr389Ala

cDNA level identifier (n.a.):

c.1165A>G

Gene level identifier:

g.63404A>G

Reference, alternative allele:

A, G

Genomic location

not available

Gene name:

SPAST

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

27

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).