Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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