Mutation details:

Protein level identifier (n.a.):

p.Pro87Ser

cDNA level identifier (n.a.):

c.259C>T

Gene level identifier:

g.6814C>T

Reference, alternative allele:

C, T

Genomic location hg(0)

11:112103901 (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:

11 compound heterozygous (11 in total).