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Varaico: Literature-Extracted Genetic Variants

Include likely false extractions

Gene:SCN3B

Variant:p.T138del1

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SCN3B

NM_001040151.2:p.T138del1

hg38:chr11:123642476 GCGT>G

Associated Papers

A novel SCN3B in-frame codon deletion in a Brugada syndrome patient: Implications for disrupted NaV1.5 function.

Sarbjit-Singh SS et al.

Journal of Molecular and Cellular Cardiology, 2025

39761910 (PubMed )

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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."