Variant ID 425
Entrez Gene ID 6323
Gene SCN1A (GeneCards)
Location hg19 2:166908463-166908463
hg38 2:166051953-166051953
Disease Dravet syndrome (view all the variants in this disease)
Method RFLP
Mutation(HGVS format) NC_000002.11:g.166908463 C>A (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Exon number 6
Position in protein 244
Amino acid changes in protein V > L
Position in cDNA 730
Changes in cDNA G > T
mRNA accession NM_001202435.1
mRNA length 6030
Reference length 243199373

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.7004
CADD Raw score (version 1.3) 5.541838 (Deleterious)
FATHMM raw prediction score 0.98643 (Tolerated)
SIFT score 0.001 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 1.45 (Tolerated)
PROVEAN score -2.93 (Deleterious)
MetaSVM score 1.115 (Deleterious)
MetaLR score 0.945 (Deleterious)
MCAP score 0.902 (Deleterious)
FitCons score 0.487 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.41
PhyloP score based on multiple alignment of 100 vertebrates 7.855
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 19.554
Deleterious probability by iFish2 0.9187 (Deleterious)
Deleterious probability by DeFine 0.966 (Deleterious)
Entrez Gene ID 6323 (NCBI Gene)
Official Gene Symbol SCN1A (GeneCards)
Number of variants in SCN1A in this database 187 (view all the variants)
Full name sodium voltage-gated channel alpha subunit 1
Band 2q24.3
Other IDs Vega: OTTHUMG00000044173
OMIM: 182389
HGNC: HGNC:10585
Ensembl: ENSG00000144285
Other names FEB3, FHM3, NAC1, SCN1, SMEI, EIEE6, FEB3A, HBSCI, GEFSP2, Nav1.1
Summary Voltage-dependent sodium channels are heteromeric complexes that regulate sodium exchange between intracellular and extracellular spaces and are essential for the generation and propagation of action potentials in muscle cells and neurons. Each sodium channel is composed of a large pore-forming, glycosylated alpha subunit and two smaller beta subunits. This gene encodes a sodium channel alpha subunit, which has four homologous domains, each of which contains six transmembrane regions. Allelic variants of this gene are associated with generalized epilepsy with febrile seizures and epileptic encephalopathy. Alternative splicing results in multiple transcript variants. The RefSeq Project has decided to create four representative RefSeq records. Three of the transcript variants are supported by experimental evidence and the fourth contains alternate 5' untranslated exons, the exact combination of which have not been experimentally confirmed for the full-length transcript. [provided by RefSeq, Oct 2015]

Individual #1

Individual ID 17054696.01 (view all the variants in this individual)
Pubmed ID 17054696
Whose mosaic mutation Mother  
Phenotype 1  
Number of affected children 2 ( male: 2; )
Disease Dravet syndrome (view all the variants in this disease)
OMIM ID 607208

Publication #1: 17054696

Pubmed ID 17054696
Title SCN1A Mutation Mosaicism in a Family with Severe Myoclonic Epilepsy in Infancy
Journal Epilepsia
Publication date 2006.01
Disease Dravet syndrome
Number of cases Female cases: 1;