Variant #0001000197 (NC_000012.11:g.52162796G>A, NM_014191.3:c.3049G>A (SCN8A))

Chromosome 12
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.52162796G>A
DNA change (hg38) -
Published as SCN8A(NM_014191.3):c.3049G>A (p.(Ala1017Thr))
ISCN -
DB-ID SCN8A_000240
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 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 13:16:32 +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.3049G>A r.(?) p.(Ala1017Thr)
SCN8A NM_014191.3 -?/. - c.3049G>A r.(?) p.(Ala1017Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.