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166848437 G/A: c.5348C>T: p.Ala1783Val: Missense

Reference genomes Human GRCh37/hg19
Genomic position 166848437
Ref/Alt G/A
Genbank transcript ID NM_001165963.1
cds change c.5348C>T
cds alteration type Non-synonymous
Zygosis Heterozygous
AA change p.Ala1783Val
AA alteration type Missense
Detection methods PCR-Sanger, MLPA, DHPLC
Known variant Known
Reference ID rs121917921
MAF in 1000G .
MAF in ExAC .
MAF in genomAD .
Exon/Intron Exon26
Protein Domain DIVS6
Inheritance De novo
Variant Classification Pathogenic
Clinical diagnosis Dravet syndrome
Gender Male
Ethnogenesis Unknown
Family history Unknown
Age of seizure onset 2 months old
Short descriptions for Cases
References Petrelli, Cristina, et al. "Early clinical features in Dravet syndrome patients with and without SCN1A mutations." Epilepsy research 99.1-2 (2012): 21-27.
co-existing variant(s)