F8 c.3712G>T ;(p.G1238C)

Variant ID: X-154158353-C-A

NM_000132.3(F8):c.3712G>T;(p.G1238C)

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:

Coagulation abnormalities of sickle cell disease: Relationship with clinical outcomes and the effect of disease modifying therapies.

Blood Reviews
Noubouossie, Denis D; Key, Nigel S NS; Ataga, Kenneth I KI
Publication Date: 2016-07

Variant appearance in text: FVIII: G1238C
PubMed Link: 26776344
Variant Present in the following documents:
  • Main text
View BVdb publication page