Mutation details:

Protein level identifier (n.a.):

p.Asp441Val

cDNA level identifier (n.a.):

c.1322A>T

Gene level identifier:

g.73267A>T

Reference, alternative allele:

A, T

Genomic location

not available

Gene name:

SPAST

Consequence:

missense

Pathogenicity scoring:

Possibly pathogenic

CADD score:

34

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).