All variants in the SCN9A gene

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     

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     
-/. - c.377+93G>T r.(=) p.(=) - - benign g.167163373C>A g.166306863C>A - - SCN9A_000011 - - - rs4443015 Germline - - - 0 - Andreas Laner
-/. - c.377+93G>T r.(=) p.(=) - - benign g.167163373C>A g.166306863C>A SCN9A(NM_002977.3):c.377+93G>T - SCN9A_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Utrecht
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