Proband information


Proband id 6656
Systematic Name
(NM_004992.3:)		 c.1157_1184del28
Protein name
(NP_004983)		 p.Leu386fs
Alternate systematic Name
(NM_001110792.1:)		 c.1193_1220del28
Alternate Protein name
(NP_001104262)		 p.(Leu398Profs*14)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153296095_153296122del28
Mutation type frameshift insertion or deletion
Domain C-term
Pathogenicity Mutation associated with disease
Evidence of Pathogenicity
Detection direct
Extent all exons
Source of DNA Blood
Carrier N
Carrier result
Other mutations
X-inactivation results
X-inactivation relatives
Gender Female
Sporadic/Familial sporadic
Phenotype-class Rett syndrome-classical
Reference :::

Matching entries in the proband database


No: Systematic Name Protein name Gender Carrier result Phenotype Proband id Reference
1 c.1157_1184del28 p.Leu386fs Female Rett syndrome-classical 6656 :::