Proband information
Proband id | 5251 |
---|---|
Systematic Name (NM_004992.3:) |
c.1408_1411del4insTG |
Protein name (NP_004983) |
p.Asn470Trpfs*16 |
Alternate systematic Name (NM_001110792.1:) |
c.1444_1447delinsTG |
Alternate Protein name (NP_001104262) |
p.(Asn482Trpfs*16) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153295868_153295871delinsCA |
Mutation type | combined frameshift insertion and deletion |
Domain | C-term |
Pathogenicity | Mutation associated with disease |
Evidence of Pathogenicity | |
Detection | direct |
Extent | not stated |
Source of DNA | blood |
Carrier | N |
Carrier result | |
Other mutations | |
X-inactivation results | |
X-inactivation relatives | |
Gender | Female |
Sporadic/Familial | sporadic |
Phenotype-class | Rett syndrome-not certain |
Reference | Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome:Chapleau, C.A., Lane, J., Kirwin, S.M., Schanen, C., Vinette, K.M.B., Stubbolo, D., MacLeod, P., Percy, A.K.:American Journal of Medical Genetics: 23696494 |
Matching entries in the proband database
No: | Systematic Name | Protein name | Gender | Carrier result | Phenotype | Proband id | Reference |
---|---|---|---|---|---|---|---|
1 | c.1408_1411del4insTG | p.Asn470Trpfs*16 | Female | Rett syndrome-not certain | 5251 | Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome:Chapleau, C.A., Lane, J., Kirwin, S.M., Schanen, C., Vinette, K.M.B., Stubbolo, D., MacLeod, P., Percy, A.K.:American Journal of Medical Genetics: 23696494 |