Variant information
Systematic Name (NM_004992.3:) |
c.1158_1198del41 |
---|---|
Protein name (NP_004983) |
p.Pro387fs |
Alternate systematic Name (NM_001110792.1:) |
c.1194_1234del41 |
Alternate Protein name (NP_001104262) |
p.(Pro399Glnfs*4) |
Genomic nomenclature (ChrX(GRCh37))(NC_000023.10:) |
g.153296081_153296121del41 |
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.1158_1198del41 | p.Pro387fs | Female | Rett syndrome-not certain | 3416 | 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 |
2 | c.1158_1198del41 | p.Pro387fs | Female | Rett syndrome-not certain | 3417 | 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 |