Variant #0000883873 (NC_000002.11:g.166930100G>T, NM_001165963.1:c.32C>A (SCN1A))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.166930100G>T
DNA change (hg38) -
Published as SCN1A(NM_001165963.3):c.32C>A (p.P11H), SCN1A(NM_001202435.3):c.32C>A (p.P11H)
ISCN -
DB-ID SCN1A_000380 See all 4 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) 1.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.32C>A r.(?) p.(Pro11His) -
SCN1A NM_006920.4 ?/. - c.32C>A r.(?) p.(Pro11His) -


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