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166848020 A/G: c.5765T>C: p.Ile1922Thr: Missense

Reference genomes Human GRCh37/hg19
Genomic position 166848020
Ref/Alt A/G
Genbank transcript ID NM_001165963.1
cds change c.5765T>C
cds alteration type Non-synonymous
Zygosis Heterozygous
AA change p.Ile1922Thr
AA alteration type Missense
Detection methods PCR-Sanger, DHPLC
Known variant Known
Reference ID rs121917981
MAF in 1000G .
MAF in ExAC .
MAF in genomAD .
Exon/Intron Exon26
Protein Domain C-terminus
Inheritance Unknown
Variant Classification Likely pathogenic
Clinical diagnosis SMEI
Gender Male
Ethnogenesis Unknown
Family history Unknown
Age of seizure onset 5 months old
Short descriptions for Cases
References Harkin, Louise A., et al. "The spectrum of SCN1A-related infantile epileptic encephalopathies." Brain 130.3 (2007): 843-852.
co-existing variant(s)