EAHAD-DB Latest News: May 2021 - New F5 DB Available

See Citing Us (below) for information on our 2020 publications describing the general EAHAD-DB programme, and the EAHAD F7 coagulation factor DB.

F5 Variants and DB Features

Variants in the gene (F5) that codes for coagulation factor V (FV) may be associated both with rare FV deficiency and bleeding, but also with more common prothrombotic (hypercoagulable) states. There are currently 209 unique variants in the F5 gene compiled within this database corresponding to 443 individual cases.

In order to help interpret their significance in real-life cases, we provide amino-acid alignments (to assist in estimating the effects of missense variants), together with information on common variants of F5. Read the Help Page for a more detailed feature description.

F5 Variants at LOVD

The basic F5 case data in this database will be mirrored at LOVD: go here for F5 at LOVD.

Simple FV Amino Acid Search

HGVS
Legacy

F5 Exon and Intron based search

Exon
Intron

Nomenclature: HGVS and Legacy  


F5 Variants - Haemorrhagic or Thrombotic?  


Acknowledgements


Citing Us


Latest Release- Version 1.3 (May 2021)  


Links to the other EAHAD-DB Databases  


Have you or someone you know been diagnosed with Factor V deficiency?  

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