Variant information


Systematic Name
(NM_004992.3:)		 c.865A>T
Protein name
(NP_004983)		 p.Lys289*
Alternate systematic Name
(NM_001110792.1:)		 c.901A>T
Alternate Protein name
(NP_001104262)		 p.(Lys301*)
Genomic nomenclature
(ChrX(GRCh37))(NC_000023.10:)		 g.153296414T>A
Mutation type Nonsense
Domain TRD
Pathogenicity Mutation associated with disease

View proband information


No: Systematic Name Protein name Gender Phenotype Proband id References View
1 c.865A>T p.Lys289* Female Rett syndrome-Classical 2105 :Cardiff, UK:: View details