Variant information
Systematic Name (NM_004992.3:) |
c.[1035A>G(;)1233C>T] |
---|---|
Protein name (NP_004983) |
p.[Lys345Lys(;)Ser411Ser] |
Alternate systematic Name (NM_001110792.1:) |
c.[1071A>G;1269C>T] |
Alternate Protein name (NP_001104262) |
p.? |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.[153296244T>C;153296046G>A] |
Mutation type | silent |
Domain | C-term |
Pathogenicity | Silent polymorphism |
View proband information
No: | Systematic Name | Protein name | Gender | Phenotype | Proband id | References | View |
---|---|---|---|---|---|---|---|
1 | c.[1035A>G(;)1233C>T] | p.[Lys345Lys(;)Ser411Ser] | Female | Rett syndrome-congenital | 4595 | Early infantile onset congenital Rett syndrome variants: Swedish experience through four decades and mutation analysis:Rajaei, S., Erlandson, A., Kyllerman, M., Albage, M., Lundstrom, I., Karrstedt, E.-L., Hagberg, B.:Journal of Child Neurology: 21212452 | View details |