Full data view for gene SCN1A

Information The variants shown are described using the transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.2134C>T r.(?) p.(Arg712Ter) - Unknown - pathogenic g.166898844G>A g.166042334G>A - - SCN1A_000296 - - - - Unknown - - - - - DNA SEQ - - ? - - - ? - - - - - - - 1 IMGAG
+/. - c.2134C>T r.(?) p.(Arg712Ter) - Unknown - pathogenic (dominant) g.166898844G>A g.166042334G>A - - SCN1A_000296 - PubMed: Froukh 2020 - - De novo - - - - - DNA SEQ, SEQ-NG - - NDD TF083 PubMed: Froukh 2020 analysis 103 families with neurodevelopmental disorders - - Jordan - - - - - 1 Johan den Dunnen
+/. - c.2134C>T r.(?) p.(Arg712*) - Unknown - pathogenic (dominant) g.166898844G>A - NM_006920:c.C2101T (R701X) - SCN1A_000296 - PubMed: Hamdan 2017 - - De novo - - - - - DNA SEQ, SEQ-NG - WGS DEE HSJ0780 PubMed: Hamdan 2017 WGS analysis 197 individuals with unexplained DEE (unaffected parents) - - Canada - - - - pharmaco-resistant seizures 1 Johan den Dunnen
+/. - c.2134C>T r.(?) p.(Arg712Ter) - Unknown - pathogenic g.166898844G>A - SCN1A(NM_001165963.4):c.2134C>T (p.R712*) - SCN1A_000296 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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