F7 c.1157A>G ;(p.H386R)

Variant ID: 13-113773144-A-G

NM_019616.3(F7):c.1157A>G;(p.H386R)

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:

Molecular Characterization of Iranian Patients with Inherited Coagulation Factor VII Deficiency.

Balkan Journal Of Medical Genetics : Bjmg
S, Shahbazi S; R, Mahdian M; K, Karimi K; A, Mashayekhi M
Publication Date: 2017-12

Variant appearance in text: F7: H386R
PubMed Link: 29876229
Variant Present in the following documents:
  • Main text
  • bjmg-20-019.pdf
View BVdb publication page