Variant #0001050854 (NC_000002.11:g.166019183C>T, NM_021007.2:c.-131514C>T (SCN2A))

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.166019183C>T
DNA change (hg38) -
Published as SCN3A(NM_006922.4):c.850G>A (p.(Asp284Asn))
ISCN -
DB-ID SCN2A_000402
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) 5.0E-5 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 2025-11-01 13:22:20 +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     
SCN3A NM_006922.3 -?/. - c.850G>A r.(?) p.(Asp284Asn)
SCN2A NM_021007.2 -?/. - c.-131514C>T r.(?) p.(=)


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