F8 c.670+1G>T

Variant ID: X-154215511-C-A

NM_000132.3(F8):c.670+1G>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


An Altered Splicing Registry Explains the Differential ExSpeU1-Mediated Rescue of Splicing Mutations Causing Haemophilia A.

Frontiers In Genetics
Balestra, Dario D; Maestri, Iva I; Branchini, Alessio A; Ferrarese, Mattia M; Bernardi, Francesco F; Pinotti, Mirko M
Publication Date: 2019

Variant appearance in text: F8: 670+1G>T
PubMed Link: 31649737
Variant Present in the following documents:
  • Main text
  • fgene-10-00974.pdf
View BVdb publication page