ClinVar Miner

Submissions for variant NM_001165963.4(SCN1A):c.4223G>A (p.Trp1408Ter) (rs794726784)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Bioinformatics, Peking University RCV000180900 SCV000221876 pathogenic Severe myoclonic epilepsy in infancy 2014-12-20 criteria provided, single submitter research
LifeCell International Pvt. Ltd RCV001527712 SCV001738771 pathogenic Generalized epilepsy with febrile seizures plus, type 2 criteria provided, single submitter clinical testing A heterozygous nonsense variation in exon 24 of the SCN1A gene (c.4223G>A) that results in a stop codon and premature truncation of the protein at codon 1408 (p.Trp1408Ter) was detected. The observed variant is not present in both the 1000 Genomes and gnomAD databases. The reference base is conserved across the species and in-silico prediction by Mutation taster is damaging. This variant has previously been reported for Dravet Syndrome by Xu X. et al., 2015. The stop gained p.Trp1408Ter in SCN1A (NM_001165963.4) has been reported to ClinVar as Pathogenic with a status of (1 stars) criteria provided, single submitter (Variation ID 189947 as of 2020-03-05). The gene SCN1A has a low rate of benign loss of function variants as indicated by a high LoF variants Z-Score of 7.90. The p.Trp1408Ter variant is a loss of function variant in the gene SCN1A, which is intolerant of Loss of Function variants, as indicated by the presence of existing pathogenic loss of function variant NP_001159435.1:p.Met1Ile and 346 others. There are 88 downstream pathogenic loss of function variants, with the furthest variant being 518 residues downstream of the variant p.Trp1408Ter. Based on the above evidence this variant has been classified as pathogenic according to the ACMG guidelines.

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