Varaico: Literature-Extracted Genetic Variants

Gene:MEIOB
Variant:p.D212N
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MEIOB

NM_001163560.3:p.D212N

Associated Papers

SIGMA leverages protein structural information to predict the pathogenicity of missense variants.

Zhao H et al.

Cell Reports Methods, 2024

38211594 (PubMed )
Supplement: mmc2.xlsx › Sheet1

Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia.

Zhu X et al.

Clinical Genetics, 2024

Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia.

Wang Y et al.

Frontiers in Genetics, 2022

Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure.

Cannarella R et al.

Asian Journal of Andrology, 0

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