Mutation Details

DNA changeProtein changeExon/intronTypeReported classificationBatemanSIFTPolyPhenConservedProtein domainRemarksLOVD ID
c.1546+2T>Cp.?Intron 12Splice siteDisease-causingn.a.Toleratedn.a.n.a. n.a.  

Patients

Family# Affected relativesClinical featuresRemarksReference
1 1 Hydrocephalus, Mental retardation 2 yrs Finckh et al. (2000)

References

YearAuthorTitleJournalVolumePagesWeblink
2000Finckh et al.Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease Am. J. Med. Genet. 9240-46 10797421