Variant information
Systematic Name (NM_004992.3:) |
c.382C>T |
---|---|
Protein name (NP_004983) |
p.Gln128* |
Alternate systematic Name (NM_001110792.1:) |
c.418C>T |
Alternate Protein name (NP_001104262) |
p.(Gln140*) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296897G>A |
Mutation type | nonsense |
Domain | MBD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.382C>T | p.Gln128* | Female | Rett syndrome-not certain | 3169 | Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update:Philippe C, Villard L, de Roux N, Raynaud M, Bonnefond JP, Pasquier L, Lesca G, Mancini J, Jonveaux P, Moncla A, Chelly J, Bienvenu T:European Journal of Medical Genetics: 16473305 | View details |
2 | c.382C>T | p.Gln128* | Female | Rett syndrome-not certain | 4911 | Genetic and epileptic features in Rett syndrome:Kim, H.J., Kim, S.H., Kim, H.D., Lee, J.S., Lee, Y.-M., Koo, K.Y., Lee, J.S., Kang, H.-C.:Yonsei Med J: 22476991 | View details |