Variant #0001000198 (NC_000012.11:g.52163117G>A, NM_014191.3:c.3370G>A (SCN8A))

Chromosome 12
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.52163117G>A
DNA change (hg38) -
Published as SCN8A(NM_001177984.2):c.3370G>A (p.(Asp1124Asn))
ISCN -
DB-ID SCN8A_000241
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN8A NM_001330260.2 ?/. - c.3370G>A r.(?) p.(Asp1124Asn)
SCN8A NM_014191.3 ?/. - c.3370G>A r.(?) p.(Asp1124Asn)


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