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.688+13T>C r.(=) p.(=) - - benign g.167160735A>G g.166304225A>G - - SCN9A_000080 - - - rs7444988 Germline - - - 0 - Andreas Laner
-/. - c.688+13T>C r.(=) p.(=) - - benign g.167160735A>G g.166304225A>G SCN9A(NM_002977.3):c.688+13T>C - SCN9A_000080 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_AMC
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