Varaico: Literature-Extracted Genetic Variants

Gene:F9
Variant:p.N36T
Back to variants list

F9

NM_000133.4:p.N36T

Associated Papers

"An integrated multitool analysis contributes elements to interpreting unclassified factor IX missense variants associated with hemophilia B": reply.

Branchini A et al.

Journal of Thrombosis and Haemostasis : Jth, 2025

Characterization of missense mutations in the signal peptide and propeptide of FIX in hemophilia B by a cell-based assay.

Gao W et al.

Blood Advances, 2020

The CDC Hemophilia B mutation project mutation list: a new online resource.

Li T et al.

Molecular Genetics & Genomic Medicine, 2013

24498619 (PubMed )
Supplement: mgg30001-0238-SD1.xlsx › CHBMP_Mutation_List
Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."