Variant information


Systematic Name
(NM_004992.3:)		 c.1099_1118del20
Protein name
(NP_004983)		 p.His367fs
Alternate systematic Name
(NM_001110792.1:)		 c.1135_1154del20
Alternate Protein name
(NP_001104262)		 p.(His379Argfs*19)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153296161_153296180del20
Mutation type Frameshift insertion or deletion
Domain C-term
Pathogenicity Mutation associated with disease

View proband information


No: Systematic Name Protein name Gender Phenotype Proband id References View
1 c.1099_1118del20 p.His367fs Female Rett syndrome-Not certain 1255 Influence of mutation type and location on phenotype in 123 patients with Rett syndrome:Huppke, P., Held, M., Hanefeld, F., Engel, W., Laccone, F.:Neuropediatrics: 12075485 View details