Full data view for gene SCN9A

Information The variants shown are described using the NM_002977.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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.596+25C>T r.(=) p.(=) - Parent #1 - benign g.167162277G>A g.166305767G>A - - SCN9A_000003 - - - rs4429487 Germline - - - 0 - DNA SEQ - - - - - - - - Germany - - 0 - - 1 Andreas Laner
?/. 5i c.596+25C>T r.(=) p.(=) - Unknown - VUS g.167162277G>A g.166305767G>A - - SCN9A_000003 - Lossin, unpublished data - - Germline - - - 0 - DNA SEQ - - erythromelalgia, primary - Lossin, unpublished data - M - United States white - 0 - - 1 Christoph Lossin
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