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Varaico: Literature-Extracted Genetic Variants

Include likely false extractions

Gene:FOXP1

Variant:p.T315_P316insFs

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FOXP1

NM_001349342.3:p.T315_P316insFs

hg38:chr3:70977930 G>GA

Associated Papers

Severe speech impairment is a distinguishing feature of FOXP1-related disorder.

Braden RO et al.

Developmental Medicine and Child Neurology, 2021

34109629 (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."