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166848341 AACTTCTCC/-: c.5436_5444delGGAGAAGTT: p.Trp1812_Phe1815delinsCys: Non-frame shift indels

Reference genomes Human GRCh37/hg19
Genomic position 166848341
Ref/Alt AACTTCTCC/-
Genbank transcript ID NM_001165963.1
cds change c.5436_5444delGGAGAAGTT
cds alteration type Non-frame shift indels
Zygosis Heterozygous
AA change p.Trp1812_Phe1815delinsCys
AA alteration type Non-frame shift indels
Detection methods PCR-Sanger, DHPLC
Known variant Unknown
Reference ID .
MAF in 1000G .
MAF in ExAC .
MAF in genomAD .
Exon/Intron Exon26
Protein Domain C-terminus
Inheritance De novo
Variant Classification Uncertain significance
Clinical diagnosis SMEI
Gender Unknown
Ethnogenesis Unknown
Family history Unknown
Age of seizure onset Unknown
Short descriptions for Cases
References Nabbout, R., et al. "Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy." Neurology 60.12 (2003): 1961-1967.
co-existing variant(s)