166848117 C/-: c.5668delG: p.Glu1890Lysfs*21: Truncation
| Reference genomes | Human GRCh37/hg19 |
|---|---|
| Genomic position | 166848117 |
| Ref/Alt | C/- |
| Genbank transcript ID | NM_001165963.1 |
| cds change | c.5668delG |
| cds alteration type | Frame shift indels |
| Zygosis | Heterozygous |
| AA change | p.Glu1890Lysfs*21 |
| AA alteration type | Truncation |
| 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) |