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.
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.1942-3dup r.spl? p.? - - likely benign g.167138330dup g.166281820dup SCN9A(NM_002977.3):c.1942-13_1942-12insT, SCN9A(NM_002977.3):c.1942-13delAinsAT, SCN9A(NM_002977.3):c.1942-3dupT - SCN9A_000144 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
-/. - c.1942-3dup r.spl? p.? - - benign g.167138330dup g.166281820dup SCN9A(NM_002977.3):c.1942-13_1942-12insT, SCN9A(NM_002977.3):c.1942-13delAinsAT, SCN9A(NM_002977.3):c.1942-3dupT - SCN9A_000144 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_AMC
Legend   How to query