Mutation details:

Protein level identifier (n.a.):

p.Gln161*

cDNA level identifier (n.a.):

c.481C>T

Gene level identifier:

g.37271C>T

Reference, alternative allele:

G, A

Genomic location hg(19)

7:94248251

Gene name:

SGCE

Consequence:

nonsense

Pathogenicity scoring:

Probably pathogenic

CADD score:

not available

Phosphorylation activity:

Positive functional evidence:

not available

Number of all included cases:

1 heterozygous (1 in total).