F8 c.787+1870C>T

Variant ID: X-154211092-G-A

NM_000132.3(F8):c.787+1870C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of deep intronic individual variants in patients with hemophilia A by next-generation sequencing of the whole factor VIII gene.

Research And Practice In Thrombosis And Haemostasis
Inaba, Hiroshi H; Shinozawa, Keiko K; Amano, Kagehiro K; Fukutake, Katsuyuki K
Publication Date: 2017-10

Variant appearance in text: F8: 787+1870C>T
PubMed Link: 30046696
Variant Present in the following documents:
  • Main text
  • RTH2-1-264.pdf
View BVdb publication page