VEGFA c.496_498delinsTGG ;(p.R166W)

Variant ID: 6-43738939-AGA-TGG

NM_003376.5(VEGFA):c.496_498delinsTGG;(p.R166W)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Von Hippel-Lindau disease: insights into oxygen sensing, protein degradation, and cancer.

The Journal Of Clinical Investigation
Kaelin, William G WG
Publication Date: 2022-09-15

Variant appearance in text: VEGF: R166W
PubMed Link: 36106637
Variant Present in the following documents:
  • jci-132-162480.pdf
View BVdb publication page



Complex cellular functions of the von Hippel-Lindau tumor suppressor gene: insights from model organisms.

Oncogene
Hsu, T T
Publication Date: 2012-05-03

Variant appearance in text: VEGF: R166W
PubMed Link: 21996733
Variant Present in the following documents:
  • Main text
View BVdb publication page



von Hippel-Lindau mutation in mice recapitulates Chuvash polycythemia via hypoxia-inducible factor-2alpha signaling and splenic erythropoiesis.

The Journal Of Clinical Investigation
Hickey, Michele M MM; Lam, Jennifer C JC; Bezman, Natalie A NA; Rathmell, W Kimryn WK; Simon, M Celeste MC
Publication Date: 2007-12

Variant appearance in text: VEGF: R166W
PubMed Link: 17992257
Variant Present in the following documents:
  • Main text
View BVdb publication page