Full data view for gene SCN9A

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

8 entries on 1 page. Showing entries 1 - 8.
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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     
-/. - c.1828C>A r.(?) p.(Pro610Thr) - Parent #1 - benign g.167141109G>T g.166284599G>T - - SCN9A_000030 - - - rs41268673 Germline - - - - - DNA SEQ - - - - - - - - Germany - - - - - 1 Andreas Laner
-/. - c.1828C>A r.(?) p.(Pro610Thr) - Unknown - benign g.167141109G>T g.166284599G>T SCN9A(NM_002977.3):c.1828C>A (p.P610T) - SCN9A_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.1828C>A r.(?) p.(Pro610Thr) - Unknown - likely benign g.167141109G>T g.166284599G>T SCN9A(NM_002977.3):c.1828C>A (p.P610T) - SCN9A_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 12 c.1828C>A r.(?) p.(Pro610Thr) L1 Unknown - pathogenic g.167141109G>T g.166284599G>T - - SCN9A_000030 - PubMed: Drenth 2005 - - Germline - - - - - DNA SEQ - - erythromelalgia, primary - PubMed: Drenth 2005 - - - - - - - - - 1 Christoph Lossin
-/. - c.1828C>A r.(?) p.(Pro610Thr) - Unknown - benign g.167141109G>T g.166284599G>T SCN9A(NM_002977.3):c.1828C>A (p.P610T) - SCN9A_000030 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.1828C>A r.(?) p.(Pro610Thr) - Parent #1 - likely benign g.167141109G>T g.166284599G>T - - SCN9A_000030 60 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs41268673 Germline - 60/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 60 Mohammed Faruq
-?/. - c.1828C>A r.(?) p.(Pro610Thr) - Both (homozygous) - likely benign g.167141109G>T g.166284599G>T - - SCN9A_000030 1 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs41268673 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+?/. - c.1828C>A r.(?) p.(Pro610Thr) - Parent #1 - VUS g.167141109G>T g.166284599G>T - - SCN9A_000030 - PubMed: Shadrina 2016 - rs41268673 Germline - - - - - DNA SEQ, SEQ-NG - WES SCA family PubMed: Shadrina 2016 4-generation family, 5 affected (5M) M - Russia - - - - - 1 Johan den Dunnen
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