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Varaico: Literature-Extracted Genetic Variants

Include likely false extractions

Gene:TPCN2

Variant:p.V675V

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TPCN2

NM_139075.4:p.V675V

hg38:chr11:69086544 A>G

Associated Papers

A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.

Kalay E et al.

Journal of Molecular Medicine (berlin, Germany), 2007

17211611 (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."