VWF c.3859A>G ;(p.R1287G)

Variant ID: 12-6128725-T-C

NM_000552.3(VWF):c.3859A>G;(p.R1287G)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Identification of pathogenic missense mutations using protein stability predictors.

Scientific Reports
Gerasimavicius, Lukas L; Liu, Xin X; Marsh, Joseph A JA
Publication Date: 2020-09-21

Variant appearance in text: VWF: R1287G
PubMed Link: 32958805
Variant Present in the following documents:
  • 41598_2020_72404_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page



Structural basis of regulation of von Willebrand factor binding to glycoprotein Ib.

The Journal Of Biological Chemistry
Blenner, Mark A MA; Dong, Xianchi X; Springer, Timothy A TA
Publication Date: 2014-02-28

Variant appearance in text: VWF: R1287G
PubMed Link: 24391089
Variant Present in the following documents:
  • Main text
View BVdb publication page



Functional display of platelet-binding VWF fragments on filamentous bacteriophage.

Plos One
Yee, Andrew A; Tan, Fen-Lai FL; Ginsburg, David D
Publication Date: 2013

Variant appearance in text: VWF: R1287G
PubMed Link: 24019925
Variant Present in the following documents:
  • Main text
View BVdb publication page