Variant #0000301868 (NC_000002.11:g.166245787C>A, NM_021007.2:c.5471C>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.166245787C>A
DNA change (hg38) g.165389277C>A
Published as SCN2A(NM_021007.3):c.5471C>A (p.A1824D)
ISCN -
DB-ID SCN2A_000162
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN3A NM_006922.3 ?/. - c.-185702G>T r.(?) p.(=)
SCN2A NM_021007.2 ?/. - c.5471C>A r.(?) p.(Ala1824Asp)


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