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VEGFA c.895G>A ;(p.E299K)
Variant ID: 6-43746236-G-A
NM_003376.5(
VEGFA
):c.895G>A;(p.E299K)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
A next-generation sequencing-based strategy combining microsatellite instability and tumor mutation burden for comprehensive molecular diagnosis of advanced colorectal cancer.
Bmc Cancer
Xiao, Jian J; Li, Wenyun W; Huang, Yan Y; Huang, Mengli M; Li, Shanshan S; Zhai, Xiaohui X; Zhao, Jing J; Gao, Chan C; Xie, Wenzhuan W; Qin, Hao H; Cai, Shangli S; Bai, Yuezong Y; Lan, Ping P; Zou, Yifeng Y
Publication Date: 2021-03-16
Variant appearance in text: VEGFA: 895G>A; E299K
PubMed Link:
33726687
Variant Present in the following documents:
12885_2021_7942_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page
Thyroid Hormones as Renal Cell Cancer Regulators.
Journal Of Signal Transduction
Szymański, Łukasz Ł; Matak, Damian D; Bartnik, Ewa E; Szczylik, Cezary C; Czarnecka, Anna M AM
Publication Date: 2016
Variant appearance in text: VEGF: E299K
PubMed Link:
27034829
Variant Present in the following documents:
Main text
View BVdb publication page