Variant information


Systematic Name c.1105delC
Protein name p.His369fs
Mutation type Frameshift insertion or deletion
Domain C-term
Pathogenicity Mutation associated with disease

Proband information


Source of DNA blood
Detection direct
Extent Exons 2-4
Evidence of Pathogenicity
Carrier status checked Not checked
Carrier result
Other mutations N
X-inactivation results
X-inactivation relatives
Gender Female
Sporadic/Familial Not known
Phenotype-class Not Known
Reference :Friez, Michael::

Matching entries in the proband database


No: Systematic Name Protein name Mutation type Domain Pathogenicity Gender Phenotype Proband id References
1 c.1105delC p.His369fs Frameshift insertion or deletion C-term Mutation associated with disease Female Not Known 1695 :Friez, Michael::
2 c.1105delC p.His369fs frameshift insertion or deletion C-term Mutation associated with disease Female Rett syndrome-classical 6670 :::