Variant #0001032463 (NC_000002.11:g.166032862G>A, NM_021007.2:c.-117835G>A (SCN2A))

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.166032862G>A
DNA change (hg38) -
Published as SCN3A(NM_006922.4):c.43C>T (p.(Arg15Cys))
ISCN -
DB-ID SCN2A_000389
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 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 2025-05-05 21:14:00 +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     
SCN3A NM_006922.3 ?/. - c.43C>T r.(?) p.(Arg15Cys)
SCN2A NM_021007.2 ?/. - c.-117835G>A r.(?) p.(=)


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