F8 c.1292T>C ;(p.L431S)

Variant ID: X-154194396-A-G

NM_000132.3(F8):c.1292T>C;(p.L431S)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Compensated pathogenic variants in coagulation factors VIII and IX present complex mapping between molecular impact and hemophilia severity.

Scientific Reports
Marín, Òscar Ò; Aguirre, Josu J; de la Cruz, Xavier X
Publication Date: 2019-07-02

Variant appearance in text: F8: L431S
PubMed Link: 31267011
Variant Present in the following documents:
  • 41598_2019_45916_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Systematic molecular analysis of hemophilia A patients from Colombia.

Genetics And Molecular Biology
Yunis, Luz Karime LK; Linares, Adriana A; Cabrera, Edgar E; Yunis, Juan J JJ
Publication Date: 2018

Variant appearance in text: FVIII: 1292T>C
PubMed Link: 30534853
Variant Present in the following documents:
  • Main text
  • 1415-4757-GMB-1678-4685-GMB-2017-0072.pdf
View BVdb publication page



Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: HEMA: L431S
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: F8: L431S
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 5
View BVdb publication page