VEGFA c.176T>C ;(p.L59P)

Variant ID: 6-43738619-T-C

NM_003376.5(VEGFA):c.176T>C;(p.L59P)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic Factors in Antiphospholipid Syndrome: Preliminary Experience with Whole Exome Sequencing.

International Journal Of Molecular Sciences
Barinotti, Alice A; Radin, Massimo M; Cecchi, Irene I; Foddai, Silvia Grazietta SG; Rubini, Elena E; Roccatello, Dario D; Sciascia, Savino S; Menegatti, Elisa E
Publication Date: 2020-12-15

Variant appearance in text: VEGFA: Leu59Pro
PubMed Link: 33333988
Variant Present in the following documents:
  • Main text
  • ijms-21-09551.pdf
View BVdb publication page



A Single-Nucleotide Polymorphism of αVβ₃ Integrin Is Associated with the Andes Virus Infection Susceptibility.

Viruses
Martínez-Valdebenito, Constanza C; Angulo, Jenniffer J; Le Corre, Nicole N; Marco, Claudia C; Vial, Cecilia C; Miquel, Juan Francisco JF; Cerda, Jaime J; Mertz, Gregory G; Vial, Pablo P; Lopez-Lastra, Marcelo M; Ferrés, Marcela M
Publication Date: 2019-02-20

Variant appearance in text: VEGF: Leu59Pro
PubMed Link: 30791508
Variant Present in the following documents:
  • Main text
  • viruses-11-00169.pdf
View BVdb publication page



Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma.

Nature Medicine
Jinnin, Masatoshi M; Medici, Damian D; Park, Lucy L; Limaye, Nisha N; Liu, Yanqiu Y; Boscolo, Elisa E; Bischoff, Joyce J; Vikkula, Miikka M; Boye, Eileen E; Olsen, Bjorn R BR
Publication Date: 2008-11

Variant appearance in text: VEGF: L59P
PubMed Link: 18931684
Variant Present in the following documents:
  • NIHMS69200-supplement-1.pdf
View BVdb publication page