CDKL5 Variant



   CSV explantation text


Variant ID: cm227

Systematic name: c.2530delC

Protein name: p.His844Ilefs*19

Alternate name(s): p.H844IfsX19, p.H844fs

Mutation type: frameshift insertion and/or deletion

Domain: regulatory C-terminal

Pathogenicity class: pathogenic variant

dbSNP ID:

First reference: Directly submitted

Comments:

Variant last updated on: 2014-10-31 04:29:20

Matching entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.2530delC p.His844Ilefs*19 Rett syndrome - classical Female Directly submitted cp464

Displaying a total number of 1 proband entries matching this variant.