c.1-?_6030+?del: Whole gene deletion

Reference genomes Human GRCh37/hg19
Genomic position -
Ref/Alt -
Genbank transcript ID NM_001165963.1
cds change c.1-?_6030+?del
cds alteration type
Zygosis Heterozygous
AA change -
AA alteration type Whole gene deletion
Detection methods PCR-Sanger
Known variant
Reference ID
MAF in 1000G
MAF in genomAD
Exon/Intron Exon1
Protein Domain
Inheritance Unknown
Variant Classification Pathogenic
Clinical diagnosis SMEI
Gender Male
Ethnogenesis Caucasian
Family history Mother: Febrile seizures; Maternal grandfather: Epilepsy
Age of seizure onset 3 months old
Short descriptions for Cases
References Suls, Arvid, et al. "Microdeletions involving the SCN1A gene may be common in SCN1A‐mutation‐negative SMEI patients." Human mutation 27.9 (2006): 914-920.
co-existing variant(s)