Mutation details:

Protein level identifier (n.a.):

p.Val163Ala

cDNA level identifier (n.a.):

c.488T>C

Gene level identifier:

g.59097T>C

Reference, alternative allele:

T, C

Genomic location hg(0)

not available

Gene name:

ATL1

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

26

Positive functional evidence:

not available

Number of all included cases:

2 heterozygous (2 in total).