FOXG1 Proband Entry



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Entry ID: fp84

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

Gender: Male

Phenotype: Not known

Other mutation: N

Chromosomal abnormality: Not known

Method of testing: direct

Source of DNA: Blood

Familial testing: No

Control screening: No

dbSNP ID:

Source: Directly submitted

Comments:

Entry last updated on: 2016-01-07 21:55:25

Similar 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

Displaying a total number of 1 proband entries.