FOXG1 Variant

   CSV explantation text

Variant ID: fm11

Systematic name: c.924G>A

Protein name: p.Trp308*

Alternate name(s):

Mutation type: nonsense

Domain: Groucho-binding domain

Pathogenicity class: pathogenic variant


First reference: Philippe, C., Amsallem, D., Fancannet, C., Lambert, L., Saunier, A., Verneau, F., Jonveaux, P. (2010) Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females. Journal of Medical Genetics 47:59-65. Pubmed ID: 19564653


Variant last updated on: 2018-06-26 10:41:54

Matching entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.924G>A p.Trp308* Not Rett syndrome - sporadic Female 19564653, Philippe, C et al (2010) fp11

Displaying a total number of 1 proband entries matching this variant.