Mutation details:

Protein level identifier (n.a.):

p.Tyr134*

cDNA level identifier (n.a.):

c.402C>A

Gene level identifier:

g.32824C>A

Reference, alternative allele:

G, T

Genomic location hg(19)

7:94252698

Gene name:

SGCE

Consequence:

nonsense

Pathogenicity scoring:

Possibly pathogenic

CADD score:

not available

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).