Mutation details:

Protein level identifier (n.a.):

p.Thr156Ile

cDNA level identifier (n.a.):

c.467C>T

Gene level identifier:

g.59076C>T

Reference, alternative allele:

C, T

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:

6 heterozygous (6 in total).

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