Variant #0000947383 (NC_000002.11:g.166032837G>A, NM_021007.2:c.-117860G>A (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.166032837G>A
DNA change (hg38) -
Published as SCN3A(NM_006922.4):c.68C>T (p.A23V)
ISCN -
DB-ID SCN2A_000347 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) 0.00012 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +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.68C>T r.(?) p.(Ala23Val)
SCN2A NM_021007.2 -?/. - c.-117860G>A r.(?) p.(=)


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