Proband information


Proband id 231
Systematic Name
(NM_004992.3:)		 c.481G>T
Protein name
(NP_004983)		 p.Gly161Trp
Alternate systematic Name
(NM_001110792.1:)		 c.517G>T
Alternate Protein name
(NP_001104262)		 p.(Gly173Trp)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153296798C>A
Mutation type Missense
Domain MBD
Pathogenicity Unknown
Evidence of Pathogenicity 100 chromosomes tested and not found in 100 chromosomes
Detection
Extent
Source of DNA
Carrier
Carrier result
Other mutations
X-inactivation results
X-inactivation relatives
Gender Unknown
Sporadic/Familial
Phenotype-class Rett syndrome-Not certain
Reference A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients:Bourdon, Violaine, Philippe, Christophe, Labrune, Orianne, Amsallem, Daniel, Arnould, Cécile, Jonveaux, Philippe:Human genetics: 11214906

Matching entries in the proband database


No: Systematic Name Protein name Gender Carrier result Phenotype Proband id Reference
1 c.481G>T p.Gly161Trp Unknown Rett syndrome-Not certain 231 A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients:Bourdon, Violaine, Philippe, Christophe, Labrune, Orianne, Amsallem, Daniel, Arnould, Cécile, Jonveaux, Philippe:Human genetics: 11214906