F8 c.*1379A>G

Variant ID: X-154064493-T-C

NM_000132.3(F8):c.*1379A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis.

Plos One
Pagliari, Maria Teresa MT; Cairo, Andrea A; Boscarino, Marco M; Mancini, Ilaria I; Pappalardo, Emanuela E; Bucciarelli, Paolo P; Martinelli, Ida I; Rosendaal, Frits R FR; Peyvandi, Flora F
Publication Date: 2021

Variant appearance in text: rs36101366
PubMed Link: 34662354
Variant Present in the following documents:
  • pone.0258675.s002.pdf
View BVdb publication page



In silico profiling of deleterious amino acid substitutions of potential pathological importance in haemophlia A and haemophlia B.

Journal Of Biomedical Science
Doss C, George Priya GP
Publication Date: 2012-03-16

Variant appearance in text: rs36101366
PubMed Link: 22423892
Variant Present in the following documents:
  • Main text
  • 1423-0127-19-30.pdf
View BVdb publication page