Proband information
Proband id | 2615 |
---|---|
Systematic Name (NM_004992.3:) |
c.904C>T |
Protein name (NP_004983) |
p.Pro302Ser |
Alternate systematic Name (NM_001110792.1:) |
c.940C>T |
Alternate Protein name (NP_001104262) |
p.(Pro314Ser) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296375G>A |
Mutation type | missense |
Domain | TRD |
Pathogenicity | Unknown |
Evidence of Pathogenicity | 200 chromosomes tested and not found in 200 chromosomes |
Detection | direct |
Extent | exons 1-4 |
Source of DNA | blood |
Carrier | N |
Carrier result | |
Other mutations | NK |
X-inactivation results | |
X-inactivation relatives | |
Gender | Female |
Sporadic/Familial | sporadic |
Phenotype-class | Rett syndrome-Classical |
Reference | Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms:Zahorakova, D., Rosipal, R., Hadac, J., Zumrova, A., Bzduch, V., Misovicova, N., Baxova, A., Zeman, J., Martasek, P.:Journal of Human Genetics: 17387578 |
Matching entries in the proband database
No: | Systematic Name | Protein name | Gender | Carrier result | Phenotype | Proband id | Reference |
---|---|---|---|---|---|---|---|
1 | c.904C>T | p.Pro302Ser | Female | Rett syndrome-Classical | 2615 | Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms:Zahorakova, D., Rosipal, R., Hadac, J., Zumrova, A., Bzduch, V., Misovicova, N., Baxova, A., Zeman, J., Martasek, P.:Journal of Human Genetics: 17387578 |