Variant #0000980350 (NC_000012.11:g.52082889A>T, NC_000012.11(NM_014191.3):c.706+256A>T (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.52082889A>T
DNA change (hg38) -
Published as SCN8A(NM_001330260.2):c.706+9A>T
ISCN -
DB-ID SCN8A_000235
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 2024-04-19 20:27:30 +02:00 (CEST)
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.706+9A>T r.(=) p.(=)
SCN8A NM_014191.3 -?/. - c.706+256A>T r.(=) p.(=)


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