Varaico: Literature-Extracted Genetic Variants

Gene:FOXP1
Variant:p.Q456*
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FOXP1

NM_001349338.3:p.Q456*

Associated Papers

Analysis of exome data in a UK cohort of 603 patients with syndromic orofacial clefting identifies causal molecular pathways.

Wilson K et al.

Human Molecular Genetics, 2023

37010288 (PubMed )
Supplement: supptables_hmg-2022-ce-00520-r1_wilson_without_id_ddad023.xlsx › S4

X-CAP improves pathogenicity prediction of stopgain variants.

Rastogi R et al.

Genome Medicine, 2022

Prospective investigation of FOXP1 syndrome.

Siper PM et al.

Molecular Autism, 2017

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