Variant #0000913882 (NC_000012.11:g.52188213T>C, NM_014191.3:c.4583T>C (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.52188213T>C
DNA change (hg38) -
Published as SCN8A(NM_014191.4):c.4583T>C (p.I1528T)
ISCN -
DB-ID SCN8A_000216
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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     
SCN8A NM_001330260.2 ?/. - c.4583T>C r.(?) p.(Ile1528Thr)
SCN8A NM_014191.3 ?/. - c.4583T>C r.(?) p.(Ile1528Thr)


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