Variant information


Systematic Name c.108_111delAGAA
Protein name p.Glu37fs
Mutation type Frameshift insertion or deletion
Domain N-term
Pathogenicity Mutation associated with disease

Proband information


Source of DNA Blood
Detection direct
Extent Exons 2-4
Evidence of Pathogenicity
Carrier status checked N
Carrier result
Other mutations N
X-inactivation results
X-inactivation relatives
Gender Female
Sporadic/Familial Not known
Phenotype-class Rett syndrome-Not certain
Reference :::

Matching entries in the proband database


No: Systematic Name Protein name Mutation type Domain Pathogenicity Gender Phenotype Proband id References
1 c.108_111delAGAA p.Glu37fs Frameshift insertion or deletion N-term Mutation associated with disease Female Rett syndrome-Not certain 1857 :Bunyan, D.::
2 c.108_111delAGAA p.Glu37fs Frameshift insertion or deletion N-term Mutation associated with disease Female Rett syndrome-Not certain 1876 :::