Variant #0000991780 (NC_000002.11:g.166909392G>A, NM_001165963.1:c.664C>T (SCN1A))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.166909392G>A
DNA change (hg38) -
Published as SCN1A(NM_001165963.4):c.664C>T (p.R222*), SCN1A(NM_001202435.2):c.664C>T (p.R222*)
ISCN -
DB-ID SCN1A_000018 See all 5 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
SCN1A NM_001165963.1 +/. - c.664C>T r.(?) p.(Arg222Ter) -
SCN1A NM_006920.4 +/. - c.664C>T r.(?) p.(Arg222Ter) -


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