Variant information
Systematic Name (NM_004992.3:) |
c.[1132_1159del28;1167_1176del10];[1132_1159del28;1167_1176del10] |
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Protein name (NP_004983) |
p.[Ala378fs];[Ala378fs] |
Alternate systematic Name (NM_001110792.1:) |
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Alternate Protein name (NP_001104262) |
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Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
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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.[1132_1159del28;1167_1176del10];[1132_1159del28;1167_1176del10] | p.[Ala378fs];[Ala378fs] | Female | Rett syndrome-not certain | 2544 | The MECP2 gene mutation screening in Rett Syndrome patients from Croatia:Matijevic, T., Knezeviv, J., Barisic, I., Resic, B., Culic, V., Pavelic, J.:Annals New York Academy of Sciences: 17341617 | View details |