Variant information


Systematic Name
(NM_004992.3:)
c.1164_1206del43
Protein name
(NP_004983)
p.Pro389fs
Alternate systematic Name
(NM_001110792.1:)
c.1200_1242del43
Alternate Protein name
(NP_001104262)
p.(Pro401Leufs*6)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)
g.153296073_153296115del43
Mutation type Frameshift insertion or deletion
Domain C-term
Pathogenicity Mutation associated with disease

View proband information


No: Systematic Name Protein name Gender Phenotype Proband id References View
1 c.1164_1206del43 p.Pro389fs Female Rett syndrome-Not certain 43 MeCP2 mutations in children with and without the phenotype of Rett Syndrome:Hoffbuhr, K., Devaney, J. M., LaFleur, B., Sirianni, N., Scacheri, C., Giron, J., Schuette, J., Innis, J., Marino, M., Philippart, M., Narayanan, V., Umansky, R., Kronn, D., Hoffman, E. P., and Naidu, S.:Neurology: 11402105 View details
2 c.1164_1206del43 p.Pro389fs Unknown Rett syndrome-Not certain 260 A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients:Bourdon, Violaine, Philippe, Christophe, Labrune, Orianne, Amsallem, Daniel, Arnould, CÚcile, Jonveaux, Philippe:Human genetics: 11214906 View details
3 c.1164_1206del43 p.Pro389fs Unknown Rett syndrome-Not certain 261 A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients:Bourdon, Violaine, Philippe, Christophe, Labrune, Orianne, Amsallem, Daniel, Arnould, CÚcile, Jonveaux, Philippe:Human genetics: 11214906 View details
4 c.1164_1206del43 p.Pro389fs Female Rett syndrome-not certain 3415 Rett syndrome from quintuple and triple deletions within the MECP2 deletion hotspot region:Lebo RV, Ikuta T, Milunsky JM, Milunsky A:Clinical Genetics: 11453972 View details