Mutation details:

Protein level identifier (n.a.):

p.Arg150Gly

cDNA level identifier (n.a.):

c.448 A>G

Gene level identifier:

g.1098A>G

Reference, alternative allele:

A, G

Genomic location hg(0)

2:73115586 (not available on ExAC)

Gene name:

SPR

Consequence:

missense

Pathogenicity scoring:

Definitely pathogenic

CADD score:

not available

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 compound heterozygous (1 in total).