Variant #0000614262 (NC_000012.11:g.52115473G>C, NM_014191.3:c.1779G>C (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.52115473G>C
DNA change (hg38) g.51721689G>C
Published as SCN8A(NM_001330260.2):c.1779G>C (p.E593D), SCN8A(NM_014191.4):c.1779G>C (p.E593D)
ISCN -
DB-ID SCN8A_000095 See all 3 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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN8A NM_014191.3 -?/. - c.1779G>C r.(?) p.(Glu593Asp)


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