Varaico: Literature-Extracted Genetic Variants

Gene:FSCN2
Variant:p.K357del1
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FSCN2

NM_012418.4:p.K357del1

Associated Papers

Aggregated Genomic Data as Cohort-Specific Allelic Frequencies can Boost Variants and Genes Prioritization in Non-Solved Cases of Inherited Retinal Dystrophies.

Iancu IF et al.

International Journal of Molecular Sciences, 2022

35955564 (PubMed )
Supplement: ijms-23-08431-s001.zip › ijms-1808225-supplementary.pdf

Prioritizing variants of uncertain significance for reclassification using a rule-based algorithm in inherited retinal dystrophies.

Iancu IF et al.

Npj Genomic Medicine, 2021

33623043 (PubMed )
Supplement: 41525_2021_182_MOESM1_ESM.pdf

The role of small in-frame insertions/deletions in inherited eye disorders and how structural modelling can help estimate their pathogenicity.

Sergouniotis PI et al.

Orphanet Journal of Rare Diseases, 2016

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