Variant #0000301863 (NC_000002.11:g.166245230T>A, NM_021007.2:c.4914T>A (SCN2A))

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.166245230T>A
DNA change (hg38) g.165388720T>A
Published as SCN2A(NM_021007.3):c.4914T>A (p.R1638=)
ISCN -
DB-ID SCN2A_000006 See all 2 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) 0.28435 View details
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.-185145A>T r.(?) p.(=)
SCN2A NM_021007.2 -/. - c.4914T>A r.(?) p.(Arg1638=)


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