Varaico: Literature-Extracted Genetic Variants

Gene:FOXL2
Variant:p.F167F
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FOXL2

NM_023067.4:p.F167F

Associated Papers

Translational and clinical comparison of whole genome and transcriptome to panel sequencing in precision oncology.

Kerle IA et al.

Npj Precision Oncology, 2025

39794422 (PubMed )
Supplement: 41698_2024_788_MOESM7_ESM.xlsx › patient_10_panel_small_variants

Mutation spectrum of fork-head transcriptional factor gene (FOXL2) in Indian Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) patients.

Kaur I et al.

The British Journal of Ophthalmology, 2011

Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).

Benayoun BA et al.

Plos One, 2010

The human FOXL2 mutation database.

Beysen D et al.

Human Mutation, 2004

Identification of novel mutations in FOXL2 associated with premature ovarian failure.

Harris SE et al.

Molecular Human Reproduction, 2002

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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."