F8 c.6853C>T ;(p.Q2285*)

Variant ID: X-154088754-G-A

NM_000132.3(F8):c.6853C>T;(p.Q2285*)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Recombinant porcine factor VIII for high-risk surgery in paediatric congenital haemophilia A with high-titre inhibitor.

Haemophilia : The Official Journal Of The World Federation Of Hemophilia
Croteau, S E SE; Abajas, Y L YL; Wolberg, A S AS; Nielsen, B I BI; Marx, G R GR; Baird, C W CW; Neufeld, E J EJ; Monahan, P E PE
Publication Date: 2017-03

Variant appearance in text: FVIII: 6853C>T
PubMed Link: 28124406
Variant Present in the following documents:
  • Main text
View BVdb publication page