F8 c.2103G>T ;(p.M701I)

Variant ID: X-154175983-C-A

NM_000132.3(F8):c.2103G>T;(p.M701I)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Comprehensive molecular characterization of pediatric radiation-induced high-grade glioma.

Nature Communications
DeSisto, John J; Lucas, John T JT; Xu, Ke K; Donson, Andrew A; Lin, Tong T; Sanford, Bridget B; Wu, Gang G; Tran, Quynh T QT; Hedges, Dale D; Hsu, Chih-Yang CY; Armstrong, Gregory T GT; Arnold, Michael M; Bhatia, Smita S; Flannery, Patrick P; Lemma, Rakeb R; Hardie, Lakotah L; Schüller, Ulrich U; Venkataraman, Sujatha S; Hoffman, Lindsey M LM; Dorris, Kathleen K; Mulcahy Levy, Jean M JM; Hankinson, Todd C TC; Handler, Michael M; Liu, Arthur K AK; Foreman, Nicholas N; Vibhakar, Rajeev R; Jones, Kenneth K; Allen, Sariah S; Zhang, Jinghui J; Baker, Suzanne J SJ; Merchant, Thomas E TE; Orr, Brent A BA; Green, Adam L AL
Publication Date: 2021-09-20

Variant appearance in text: F8: M701I
PubMed Link: 34545084
Variant Present in the following documents:
  • 41467_2021_25709_MOESM12_ESM.xlsx, sheet 1
View BVdb publication page



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: FVIII: M701I
PubMed Link: 31267011
Variant Present in the following documents:
  • 41598_2019_45916_MOESM2_ESM.xlsx, sheet 1
  • 41598_2019_45916_MOESM3_ESM.xlsx, sheet 1
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: M701I
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: M701I
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 5
View BVdb publication page



VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population.

Blood
Bellissimo, Daniel B DB; Christopherson, Pamela A PA; Flood, Veronica H VH; Gill, Joan Cox JC; Friedman, Kenneth D KD; Haberichter, Sandra L SL; Shapiro, Amy D AD; Abshire, Thomas C TC; Leissinger, Cindy C; Hoots, W Keith WK; Lusher, Jeanne M JM; Ragni, Margaret V MV; Montgomery, Robert R RR
Publication Date: 2012-03-01

Variant appearance in text: FVIII: M701I
PubMed Link: 22197721
Variant Present in the following documents:
  • Main text
View BVdb publication page