Variant #0000883872 (NC_000002.11:g.166915118A>G, NM_001165963.1:c.345T>C (SCN1A))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.166915118A>G
DNA change (hg38) -
Published as SCN1A(NM_001165963.1):c.345T>C (p.(Asn115=)), SCN1A(NM_001165963.3):c.345T>C (p.N115=)
ISCN -
DB-ID SCN1A_000026 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) 0.00712 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.345T>C r.(?) p.(Asn115=) -
SCN1A NM_006920.4 -/. - c.345T>C r.(?) p.(Asn115=) -


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