VWF c.5620+19T>G

Variant ID: 12-6122628-A-C

NM_000552.3(VWF):c.5620+19T>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Fragmentation patterns and personalized sequencing of cell-free DNA in urine and plasma of glioma patients.

Embo Molecular Medicine
Mouliere, Florent F; Smith, Christopher G CG; Heider, Katrin K; Su, Jing J; van der Pol, Ymke Y; Thompson, Mareike M; Morris, James J; Wan, Jonathan C M JCM; Chandrananda, Dineika D; Hadfield, James J; Grzelak, Marta M; Hudecova, Irena I; Couturier, Dominique-Laurent DL; Cooper, Wendy W; Zhao, Hui H; Gale, Davina D; Eldridge, Matthew M; Watts, Colin C; Brindle, Kevin K; Rosenfeld, Nitzan N; Mair, Richard R
Publication Date: 2021-08-09

Variant appearance in text: VWF: 5620+19T>G
PubMed Link: 34291583
Variant Present in the following documents:
  • EMMM-13-e12881-s010.xlsx, sheet 1
  • EMMM-13-e12881-s004.xlsx, sheet 1
View BVdb publication page