Varaico: Literature-Extracted Genetic Variants

Gene:F2
Variant:p.R608R
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F2

NM_000506.5:p.R608R

Associated Papers

SyMetrics: an integrated machine learning model for evaluating the pathogenicity of synonymous variants in the human genome.

Bundalian L et al.

Nar Genomics and Bioinformatics, 2026

Synonymous variants that disrupt messenger RNA structure are significantly constrained in the human population.

Gaither JBS et al.

Gigascience, 2021

The Silence Speaks, but We Do Not Listen: Synonymous c.1824C>T Gene Variant in the Last Exon of the Prothrombin Gene as a New Prothrombotic Risk Factor.

Pruner I et al.

Clinical Chemistry, 2020

Prothrombin 3'end Gene Variants in Patients With Sporadic Colon Adenocarcinoma.

Cumbo M et al.

Anticancer Research, 2019

Prothrombin 3'end gene variants in isolated pulmonary embolism--the first report of FIIc.*64_*66del and FIIc.*303T>C variants.

Gvozdenov M et al.

Acta Cardiologica, 2015

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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."