VWF c.2279G>T ;(p.R760L)

Variant ID: 12-6155891-C-A

NM_000552.3(VWF):c.2279G>T;(p.R760L)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Intratumoral heterogeneity as a predictive biomarker in anti-PD-(L)1 therapies for non-small cell lung cancer.

Molecular Cancer
Fang, Wenfeng W; Jin, Haoxuan H; Zhou, Huaqiang H; Hong, Shaodong S; Ma, Yuxiang Y; Zhang, Yaxiong Y; Su, Xiaofan X; Chen, Longyun L; Yang, Yunpeng Y; Xu, Shengqiang S; Liao, Yuwei Y; He, Yuming Y; Zhao, Hongyun H; Huang, Yan Y; Gao, Zhibo Z; Zhang, Li L
Publication Date: 2021-02-23

Variant appearance in text: VWF: 2279G>T; R760L
PubMed Link: 33622313
Variant Present in the following documents:
  • 12943_2021_1331_MOESM3_ESM.xlsx, sheet 4
  • 12943_2021_1331_MOESM3_ESM.xlsx, sheet 8
View BVdb publication page



Next-generation sequencing identifies rare variants associated with Noonan syndrome.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Chen, Peng-Chieh PC; Yin, Jiani J; Yu, Hui-Wen HW; Yuan, Tao T; Fernandez, Minerva M; Yung, Christina K CK; Trinh, Quang M QM; Peltekova, Vanya D VD; Reid, Jeffrey G JG; Tworog-Dube, Erica E; Morgan, Margaret B MB; Muzny, Donna M DM; Stein, Lincoln L; McPherson, John D JD; Roberts, Amy E AE; Gibbs, Richard A RA; Neel, Benjamin G BG; Kucherlapati, Raju R
Publication Date: 2014-08-05

Variant appearance in text: VWF: R760L
PubMed Link: 25049390
Variant Present in the following documents:
  • Main text
View BVdb publication page