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166848111 G/A: c.5674C>T: p.Arg1892*: Truncation

Reference genomes Human GRCh37/hg19
Genomic position 166848111
Ref/Alt G/A
Genbank transcript ID NM_001165963.1
cds change c.5674C>T
cds alteration type Nonsense
Zygosis Heterozygous
AA change p.Arg1892*
AA alteration type Truncation
Detection methods PCR-Sanger, MLPA
Known variant Known
Reference ID rs794726739
MAF in 1000G .
MAF in ExAC .
MAF in genomAD .
Exon/Intron Exon26
Protein Domain C-terminus
Inheritance De novo
Variant Classification Pathogenic
Clinical diagnosis SMEI
Gender Male
Ethnogenesis Unknown
Family history Unknown
Age of seizure onset Unknown
Short descriptions for Cases
References Wang, Ji-wen, et al. "Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy." Epilepsy research 102.3 (2012): 195-200.
co-existing variant(s)