Proband information
Proband id | 2866 |
---|---|
Systematic Name (NM_004992.3:) |
c.28G>C |
Protein name (NP_004983) |
p.Glu10Gln |
Alternate systematic Name (NM_001110792.1:) |
c.64G>C |
Alternate Protein name (NP_001104262) |
p.(Glu22Gln) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153298007C>G |
Mutation type | missense |
Domain | N-term |
Pathogenicity | Unknown |
Evidence of Pathogenicity | |
Detection | DHPLC |
Extent | exons 3 and 4 |
Source of DNA | not known |
Carrier | N |
Carrier result | |
Other mutations | NK |
X-inactivation results | |
X-inactivation relatives | |
Gender | Female |
Sporadic/Familial | sporadic |
Phenotype-class | Rett syndrome-forme fruste |
Reference | Rett syndrome in adolescent and adult females:Smeets, E., Schollen, E., Moog, U., Matthijs, G., Herbergs, J., Smeets, H., Curfs, L., Schrander-Stumpel, C., Fryns, J.P.:American Journal of Medical Genetic: 12966523 |
Matching entries in the proband database
No: | Systematic Name | Protein name | Gender | Carrier result | Phenotype | Proband id | Reference |
---|---|---|---|---|---|---|---|
1 | c.28G>C | p.Glu10Gln | Female | Rett syndrome-forme fruste | 2866 | Rett syndrome in adolescent and adult females:Smeets, E., Schollen, E., Moog, U., Matthijs, G., Herbergs, J., Smeets, H., Curfs, L., Schrander-Stumpel, C., Fryns, J.P.:American Journal of Medical Genetic: 12966523 |