Variant information


Systematic Name
(NM_004992.3:)		 c.470dupT
Protein name
(NP_004983)		 p.Thr158fs
Alternate systematic Name
(NM_001110792.1:)		 c.506dupT
Alternate Protein name
(NP_001104262)		 p.(Thr170Hisfs*17)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153296809dupA
Mutation type Frameshift insertion or deletion
Domain MBD
Pathogenicity Mutation associated with disease

View proband information


No: Systematic Name Protein name Gender Phenotype Proband id References View
1 c.470dupT p.Thr158fs Female Rett syndrome-Not certain 1839 :Bunyan, D.:: View details