Variant #0000991750 (NC_000002.11:g.166027028T>C, NM_021007.2:c.-123669T>C (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.166027028T>C
DNA change (hg38) -
Published as SCN3A(NM_006922.3):c.295A>G (p.(Ile99Val)), SCN3A(NM_006922.4):c.295A>G (p.I99V)
ISCN -
DB-ID SCN3A_000021 See all 4 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) 3.0E-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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN3A NM_006922.3 -?/. - c.295A>G r.(?) p.(Ile99Val)
SCN2A NM_021007.2 -?/. - c.-123669T>C r.(?) p.(=)


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