Mutation details:

Protein level identifier (n.a.):

p.Val56Met

cDNA level identifier (n.a.):

c.166G>A

Gene level identifier:

g.3846G>A

Reference, alternative allele:

G, A

Genomic location hg(0)

11:112100933 (not available on ExAC)

Gene name:

PTS

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

not available

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

5 compound heterozygous (5 in total).