Varaico: Literature-Extracted Genetic Variants

Gene:F8
Variant:p.G2013R
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F8

NM_000132.4:p.G2013R

Associated Papers

All exons are not created equal-exon vulnerability determines the effect of exonic mutations on splicing.

Holm LL et al.

Nucleic Acids Research, 2024

38324470 (PubMed )
Supplement: gkae077_supplemental_files.zip › supplementary_tables.xlsx › Supplementary_table_S1_-_ESM_DB

Prediction of hemophilia A severity using a small-input machine-learning framework.

Lopes TJS et al.

Npj Systems Biology and Applications, 2021

34035274 (PubMed )
Supplement: 41540_2021_183_MOESM2_ESM.xlsx › Training_Set

Compensated pathogenic variants in coagulation factors VIII and IX present complex mapping between molecular impact and hemophilia severity.

Marín Ò et al.

Scientific Reports, 2019

31267011 (PubMed )
Supplement: 41598_2019_45916_MOESM2_ESM.xlsx › Variants_used

Recurrent and novel disease-causing F8 variants in boys with severe haemophilia A in Poland.

Janczar S et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia, 2019

Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activity.

Donadon I et al.

Haematologica, 2018

Hemophilia A: different phenotypes may be explained by multiple and variable effects of the causative mutation in the F8 gene.

Castaman G

Haematologica, 2018

Detection of F8 mutations in carriers and patients with severe hemophilia A. Identification of a novel mutation.

López-Vásquez L et al.

Investigacion Clinica, 2016

Detection of new mutations and molecular pathology of mild and moderate haemophilia A patients from southern Brazil.

Rosset C et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia, 2013

Identification of factor VIII gene mutations in patients with severe haemophilia A in Venezuela: identification of seven novel mutations.

Albánez S et al.

Haemophilia : the Official Journal of the World Federation of Hemophilia, 2011

Factor VIII (FVIII) gene mutations in 120 patients with hemophilia A: detection of 26 novel mutations and correlation with FVIII inhibitor development.

Repessé Y et al.

Journal of Thrombosis and Haemostasis : Jth, 2007

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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."