F8 c.4433T>G ;(p.V1478G)

Variant ID: X-154157632-A-C

NM_000132.3(F8):c.4433T>G;(p.V1478G)

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:

Complexity and diversity of F8 genetic variations in the 1000 genomes.

Journal Of Thrombosis And Haemostasis : Jth
Li, J N JN; Carrero, I G IG; Dong, J F JF; Yu, F L FL
Publication Date: 2015-11

Variant appearance in text: F8: V1478G
PubMed Link: 26383047
Variant Present in the following documents:
  • Main text
View BVdb publication page