Full data view for gene SCN9A

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     

Allele     

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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 25 c.4462C>T r.(?) p.(Arg1488*) L3 Unknown - pathogenic g.167060878G>A g.166204368G>A - - SCN9A_000071 - PubMed: Goldberg 2007 - - Germline - - - - - DNA SEQ - - CIP;HSAN2D - PubMed: Goldberg 2007 - - - United States - - - - - 1 Christoph Lossin
+/. 25 c.4462C>T r.(4462c>u) p.(Arg1488*) - Both (homozygous) - pathogenic g.167060878G>A g.166204368G>A - - SCN9A_000071 - - ClinVar-245799 rs187558439 Germline - - - - - DNA SEQ-NG whole blood - CIP;HSAN2D 1 (YA) PubMed: Danziger 2006 patient 1 (YA) in table 1 F yes France - >44y - - - 1 Wen He
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