Variant information
Systematic Name (NM_004992.3:) |
c.1160C>T |
---|---|
Protein name (NP_004983) |
p.Pro387Leu |
Alternate systematic Name (NM_001110792.1:) |
c.1196C>T |
Alternate Protein name (NP_001104262) |
p.(Pro399Leu) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296119G>A |
Mutation type | Missense |
Domain | C-term |
Pathogenicity | Unknown |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.1160C>T | p.Pro387Leu | Male | Not Rett synd. | 1022 | MECP2 is highly mutated in X-linked mental retardation:Couvert, Philippe, Bienvenu, Thierry, Aquaviva, Cecile, Poirier, Karine, Moraine, Claude, Gendrot, Chantal, Verloes, Alain, Andrès, Christian, Le Fevre, Anne Celine, Souville, Isabelle, Steffann, Julie, des Portes, Vincent, Ropers, Hans-Hilger, Yntema, Helger G., Fryns, Jean-Pierre, Briault, Sylvain, Chelly, Jamel and Cherif, Beldjord:Human Molecular Genetics: 11309367 | View details |