Variant information


Systematic Name
(NM_004992.3:)		 c.1160_1180del21
Protein name
(NP_004983)		 p.Pro387_Glu394delinsGln
Alternate systematic Name
(NM_001110792.1:)		 c.1196_1216del21
Alternate Protein name
(NP_001104262)		 p.(Pro399_Glu406delinsGln)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153296099_153296119del21
Mutation type in-frame insertion or deletion
Domain C-term
Pathogenicity Unknown

View proband information


No: Systematic Name Protein name Gender Phenotype Proband id References View
1 c.1160_1180del21 p.Pro387_Glu394delinsGln Female Rett syndrome-classical 2952 Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome; a cohort of 171 cases:Kammoun, F., de Roux, N, Boespflug-Tanguy, O., Vallée, L, seng, R., Tardieu, M., Landrieu, P.:J Med Genet: 15173251 View details
2 c.1160_1180del21 p.Pro387_Glu394delinsGln Female Rett syndrome-not certain 3513 Spectrum of MECP2 mutations in Rett syndrome:Bienvenu T, Villard L, de Roux N, Bourdon V, Fontes M, Beldjord C, Tardieu M, Jonveaux P, Chelly J:Genetic testing: 12180070 View details