Mutation details:

Protein level identifier (n.a.):

p.Thr614Ile

cDNA level identifier (n.a.):

c.1841C>T

Gene level identifier:

g.90876C>T

Reference, alternative allele:

C, T

Genomic location

not available

Gene name:

SPAST

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

22

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

16 heterozygous (16 in total).