Mutation details:

Protein level identifier (n.a.):

p.Pro123Ser

cDNA level identifier (n.a.):

c.367C>T

Gene level identifier:

g.7120C>T

Reference, alternative allele:

C, T

Genomic location hg(0)

11:112104207 (not available on ExAC)

Gene name:

PTS

Consequence:

missense

Pathogenicity scoring:

Probably pathogenic

CADD score:

not available

Positive functional evidence:

not available

Number of all included cases:

2 homozygous (2 in total).

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