Proband information


Proband id 6641
Systematic Name
(NM_004992.3:)
c.226delG
Protein name
(NP_004983)
p.Glu76fs
Alternate systematic Name
(NM_001110792.1:)
c.262delG
Alternate Protein name
(NP_001104262)
p.(Glu88Lysfs*49)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)
g.153297809delC
Mutation type frameshift insertion or deletion
Domain MBD
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.226delG p.Glu76fs Female Rett syndrome-classical 6641 :::