All variants in the SCN9A gene

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

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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     

Owner     
+/. 4 c.406A>G r.(?) p.(Ile136Val) D1/S1 - pathogenic g.167163081T>C g.166306571T>C - - SCN9A_000013 - PubMed: Cheng 2008 - - Germline - - - 0 - Christoph Lossin
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