VEGFA c.963-112G>A

Variant ID: 6-43748357-G-A

NM_003376.5(VEGFA):c.963-112G>A

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics
Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F
Publication Date: 2021

Variant appearance in text: VEGFA: 963-112G>A; rs3025017
PubMed Link: 34054912
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Mutational landscape and genetic signatures of cell-free DNA in tumour-induced osteomalacia.

Journal Of Cellular And Molecular Medicine
Wu, Nan N; Zhang, Zhen Z; Zhou, Xi X; Zhao, Hengqiang H; Ming, Yue Y; Wu, Xue X; Zhang, Xian X; Yang, Xin-Zhuang XZ; Zhou, Meng M; Bao, Hua H; Chen, Weisheng W; Wu, Yong Y; Liu, Sen S; Wang, Huizi H; Niu, Yuchen Y; Li, Yalun Y; Zheng, Yu Y; Shao, Yang Y; Gao, Na N; Yang, Ying Y; Liu, Ying Y; Li, Wenli W; Liu, Jia J; Zhang, Na N; Yang, Xu X; Xu, Yuan Y; Li, Mei M; Sun, Yingli Y; Su, Jianzhong J; Zhang, Jianguo J; Xia, Weibo W; Qiu, Guixing G; Liu, Yong Y; Liu, Jiaqi J; Wu, Zhihong Z
Publication Date: 2020-05

Variant appearance in text: VEGFA: 932+2084G>A
PubMed Link: 32277576
Variant Present in the following documents:
  • JCMM-24-4931-s010.xlsx, sheet 1
View BVdb publication page



Frequent mutation of hypoxia-related genes in persistent pulmonary hypertension of the newborn.

Respiratory Research
Wang, Mingbang M; Zhuang, Deyi D; Mei, Mei M; Ma, Haiyan H; Li, Zixiu Z; He, Fusheng F; Cheng, Guoqiang G; Lin, Guang G; Zhou, Wenhao W
Publication Date: 2020-02-13

Variant appearance in text: rs3025017
PubMed Link: 32054482
Variant Present in the following documents:
  • 12931_2020_1314_MOESM1_ESM.xlsx, sheet 7
View BVdb publication page



Relationship of common variants in VEGFA gene with osteonecrosis of the femoral head: A Han Chinese population based association study.

Scientific Reports
Ma, Wenlong W; Xin, Kun K; Chen, Ke K; Tang, Hongtao H; Chen, Honggan H; Zhi, Liqiang L; Liu, Hongliang H
Publication Date: 2018-11-01

Variant appearance in text: rs3025017
PubMed Link: 30385772
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multilocus genetic risk score for diabetic retinopathy in the Han Chinese population of Taiwan.

Scientific Reports
Liao, Wen-Ling WL; Lin, Jang-Ming JM; Chen, Wen-Lu WL; Hsieh, Ming-Chia MC; Wu, Chia-Ming CM; Chang, Ya-Wen YW; Huang, Yu-Chuen YC; Tsai, Fuu-Jen FJ
Publication Date: 2018-09-28

Variant appearance in text: rs3025017
PubMed Link: 30266984
Variant Present in the following documents:
  • 41598_2018_32916_MOESM1_ESM.pdf
View BVdb publication page



Genetics of VEGF serum variation in human isolated populations of cilento: importance of VEGF polymorphisms.

Plos One
Ruggiero, Daniela D; Dalmasso, Cyril C; Nutile, Teresa T; Sorice, Rossella R; Dionisi, Laura L; Aversano, Mario M; Bröet, Philippe P; Leutenegger, Anne-Louise AL; Bourgain, Catherine C; Ciullo, Marina M
Publication Date: 2011-02-09

Variant appearance in text: rs3025017
PubMed Link: 21347390
Variant Present in the following documents:
  • Main text
  • pone.0016982.pdf
View BVdb publication page