Variant #0000923335 (NC_000002.11:g.166911203A>G, NM_001165963.1:c.547T>C (SCN1A))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.166911203A>G
DNA change (hg38) -
Published as SCN1A(NM_001165963.4):c.547T>C (p.F183L)
ISCN -
DB-ID SCN1A_000533
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +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.547T>C r.(?) p.(Phe183Leu) -
SCN1A NM_006920.4 +?/. - c.547T>C r.(?) p.(Phe183Leu) -


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