Proband information


Proband id 2098
Systematic Name
(NM_004992.3:)		 c.1097_1203del107
Protein name
(NP_004983)		 p.His366fs
Alternate systematic Name
(NM_001110792.1:)		 c.1133_1239del107
Alternate Protein name
(NP_001104262)		 p.(His378Profs*3)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153296076_153296182del107
Mutation type Frameshift insertion or deletion
Domain C-term
Pathogenicity Mutation associated with disease
Evidence of Pathogenicity
Detection Not known
Extent Exons 2-4 (at least)
Source of DNA Blood or skin
Carrier NC
Carrier result
Other mutations N
X-inactivation results
X-inactivation relatives
Gender Female
Sporadic/Familial Not known
Phenotype-class Rett syndrome-Classical
Reference :Cardiff, UK::

Matching entries in the proband database


No: Systematic Name Protein name Gender Carrier result Phenotype Proband id Reference
1 c.1097_1203del107 p.His366fs Female Rett syndrome-Classical 2098 :Cardiff, UK::