Variant information
Systematic Name (NM_004992.3:) |
c.455C>T |
---|---|
Protein name (NP_004983) |
p.Pro152Leu |
Alternate systematic Name (NM_001110792.1:) |
c.491C>T |
Alternate Protein name (NP_001104262) |
p.(Pro164Leu) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296824G>A |
Mutation type | missense |
Domain | MBD |
Pathogenicity | Mutation associated with disease |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.455C>T | p.Pro152Leu | Female | Not Rett synd. | 7002 | Identification of autism-related MECP2 mutations by whole-exome sequencing and functional validation:Zhu Wen, Tian-Lin Cheng, Gai-zhi Li, Shi-Bang Sun, Shun-Ying Yu, Yi Zhang, Ya-Song Du and Zilong Qiu:Molecular Autism: 28785396 | View details |