Proband information


Proband id 2091
Systematic Name
(NM_004992.3:)		 c.617delG
Protein name
(NP_004983)		 p.Gly206fs
Alternate systematic Name
(NM_001110792.1:)		 c.653delG
Alternate Protein name
(NP_001104262)		 p.(Gly218Valfs*4)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153296662delC
Mutation type Frameshift insertion or deletion
Domain Inter-domain region
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.617delG p.Gly206fs Female Rett syndrome-Classical 2091 :Cardiff, UK::