166900364 T/TGTTGC: c.1857_1858insGCAAC: p.Ser620Alafs*5: Truncation

Reference genomes Human GRCh37/hg19
Genomic position 166900364
Genbank transcript ID NM_001165963.1
cds change c.1857_1858insGCAAC
cds alteration type Frame shift indels
Zygosis Heterozygous
AA change p.Ser620Alafs*5
AA alteration type Truncation
Detection methods PCR-Sanger, DHPLC, MLPA
Known variant Unknown
Reference ID .
MAF in 1000G .
MAF in ExAC .
MAF in genomAD .
Exon/Intron Exon11
Protein Domain DIDII linker
Inheritance De novo
Variant Classification Uncertain significance
Clinical diagnosis SMEB
Gender Female
Ethnogenesis Unknown
Family history Present
Age of seizure onset 3 months old
Short descriptions for Cases
References Marini, Carla, et al. "Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities." Epilepsia 48.9 (2007): 1678-1685.
co-existing variant(s)