Variant #0000301771 (NC_000002.11:g.166930064G>A, NM_001165963.1:c.68C>T (SCN1A))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.166930064G>A
DNA change (hg38) g.166073554G>A
Published as SCN1A(NM_001165963.3):c.68C>T (p.A23V), SCN1A(NM_001165963.4):c.68C>T (p.A23V)
ISCN -
DB-ID SCN1A_000274 See all 2 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) 0.00036 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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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.68C>T r.(?) p.(Ala23Val) -
SCN1A NM_006920.4 -?/. - c.68C>T r.(?) p.(Ala23Val) -


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