F7 c.845C>T ;(p.A282V)

Variant ID: 13-113772832-C-T

NM_019616.3(F7):c.845C>T;(p.A282V)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Whole-exome sequencing analyses in a Saudi Ischemic Stroke Cohort reveal association signals, and shows polygenic risk scores are related to Modified Rankin Scale Risk.

Functional & Integrative Genomics
Alkhamis, Fahad A FA; Alabdali, Majed M MM; Alsulaiman, Abdulla A AA; Alamri, Abdullah S AS; Alali, Rudaynah R; Akhtar, Mohammed S MS; Alsalman, Sadiq A SA; Cyrus, Cyril C; Albakr, Aishah I AI; Alduhalan, Anas S AS; Gandla, Divya D; Al-Romaih, Khaldoun K; Abouelhoda, Mohamed M; Loza, Bao-Li BL; Keating, Brendan B; Al-Ali, Amein K AK
Publication Date: 2023-03-27

Variant appearance in text: F7: 845C>T; Ala282Val; rs121964931
PubMed Link: 36973604
Variant Present in the following documents:
  • 10142_2023_1039_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Lethal variants in humans: lessons learned from a large molecular autopsy cohort.

Genome Medicine
Shamseldin, Hanan E HE; AlAbdi, Lama L; Maddirevula, Sateesh S; Alsaif, Hessa S HS; Alzahrani, Fatema F; Ewida, Nour N; Hashem, Mais M; Abdulwahab, Firdous F; Abuyousef, Omar O; Kuwahara, Hiroyuki H; Gao, Xin X; , ; Alkuraya, Fowzan S FS
Publication Date: 2021-10-13

Variant appearance in text: F7: 845C>T; Ala282Val
PubMed Link: 34645488
Variant Present in the following documents:
  • 13073_2021_973_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Lethal variants in humans: lessons learned from a large molecular autopsy cohort.

Genome Medicine
Shamseldin, Hanan E HE; AlAbdi, Lama L; Maddirevula, Sateesh S; Alsaif, Hessa S HS; Alzahrani, Fatema F; Ewida, Nour N; Hashem, Mais M; Abdulwahab, Firdous F; Abuyousef, Omar O; Kuwahara, Hiroyuki H; Gao, Xin X; , ; Alkuraya, Fowzan S FS
Publication Date: 2021-10-13

Variant appearance in text: F7: 845C>T; Ala282Val
PubMed Link: 34645488
Variant Present in the following documents:
  • 13073_2021_973_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Molecular classification of blood and bleeding disorder genes.

Npj Genomic Medicine
Baz, Batoul B; Abouelhoda, Mohamed M; Owaidah, Tarek T; Dasouki, Majed M; Monies, Dorota D; Al Tassan, Nada N
Publication Date: 2021-07-16

Variant appearance in text: rs121964931
PubMed Link: 34272389
Variant Present in the following documents:
  • 41525_2021_228_MOESM1_ESM.pdf
View BVdb publication page



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: A282V
PubMed Link: 29876229
Variant Present in the following documents:
  • Main text
  • bjmg-20-019.pdf
View BVdb publication page



Genetic variation in human drug-related genes.

Genome Medicine
Schärfe, Charlotta Pauline Irmgard CPI; Tremmel, Roman R; Schwab, Matthias M; Kohlbacher, Oliver O; Marks, Debora Susan DS
Publication Date: 2017-12-22

Variant appearance in text: rs121964931
PubMed Link: 29273096
Variant Present in the following documents:
  • 13073_2017_502_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page