Variant information


Systematic Name
(NM_004992.3:)		 c.819delG
Protein name
(NP_004983)		 p.Ser274fs
Alternate systematic Name
(NM_001110792.1:)		 c.855delG
Alternate Protein name
(NP_001104262)		 p.(Ser286Valfs*15)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153296460delC
Mutation type frameshift insertion or deletion
Domain TRD
Pathogenicity Mutation associated with disease

View proband information


No: Systematic Name Protein name Gender Phenotype Proband id References View
1 c.819delG p.Ser274fs Female Not Known 4105 Mutation analysis in Rett syndrome:Milunsky, J.M., Lebo, R.V., Ikuta, T., Maher, T.A., Haverty, C.E., Milunsky, A.:Genetic Testing: 11960578 View details