All variants in the SCN9A gene

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

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

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.2072-14C>T r.(=) p.(=) - - benign g.167137119G>A g.166280609G>A - - SCN9A_000168 - - - rs6432893 Germline - - - 0 - Andreas Laner
-/. - c.2072-14C>T r.(=) p.(=) - - benign g.167137119G>A g.166280609G>A SCN1A-AS1(NR_110260.1):n.1029+3362G>A, SCN9A(NM_002977.3):c.2072-14C>T - SCN9A_000168 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_AMC
-/. - c.2072-14C>T r.(=) p.(=) - - benign g.167137119G>A g.166280609G>A SCN1A-AS1(NR_110260.1):n.1029+3362G>A, SCN9A(NM_002977.3):c.2072-14C>T - SCN9A_000168 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
-/. - c.2072-14C>T r.(=) p.(=) - - benign g.167137119G>A g.166280609G>A SCN1A-AS1(NR_110260.1):n.1029+3362G>A, SCN9A(NM_002977.3):c.2072-14C>T - SCN9A_000168 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Utrecht
Legend   How to query