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Varaico: Literature-Extracted Genetic Variants

Include likely false extractions

Gene:CLDN14

Variant:p.S14fs

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CLDN14

NM_001146079.2:p.S14fs

hg38:chr21:36461656 GCT>N

Associated Papers

Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.

Mohseni M et al.

Clinical Genetics, 2021

33713422 (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."