Varaico: Literature-Extracted Genetic Variants

Gene:SCN10A
Variant:p.R497C
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SCN10A

NM_006514.4:p.R497C

Associated Papers

Genetic Analysis of SCN11A, SCN10A, and SCN9A in Familial Episodic Pain Syndrome (FEPS) in Japan and Proposal of Clinical Diagnostic Criteria.

Noguchi A et al.

International Journal of Molecular Sciences, 2024

Cardiac arrhythmia and epilepsy genetic variants in sudden unexpected death in epilepsy.

Aschner A et al.

Frontiers in Neurology, 2024

Genetic Profiling of Sodium Channels in Diabetic Painful and Painless and Idiopathic Painful and Painless Neuropathies.

Almomani R et al.

International Journal of Molecular Sciences, 2023

Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene.

Patowary A et al.

Translational Psychiatry, 2019

30664616 (PubMed )
Supplement: 41398_2018_343_MOESM3_ESM.xlsx › All_Variants
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."