FOXG1 Variant



Variant ID: fm61

Systematic name: c.505_506delGGinsT

Protein name: p.Gly169Serfs*23

Alternate name(s):

Mutation type: frameshift insertion and/or deletion

Domain: Inter domain region

Pathogenicity class: pathogenic variant

dbSNP ID:

First reference: Directly submitted

Comments:

Variant last updated on: 2016-01-07 21:55:04

Matching entries in the proband database

cDNA name Protein name Phenotype Gender Reference Proband ID
c.505_506delGGinsT p.Gly169Serfs*23 Rett syndrome - sporadic Male 21441262, Kortum, F. et al (2011) fp22
c.505_506delGGinsT p.Gly169Serfs*23 Not known Male Directly submitted fp84

Displaying a total number of 2 proband entries matching this variant.