BRAF c.1795_1800delinsCTCCCT ;(p.T599_V600delinsLP)

Variant ID: 7-140453135-CACTGT-AGGGAG

NM_004333.4(BRAF):c.1795_1800delinsCTCCCT;(p.T599_V600delinsLP)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Prognostic value of genetic aberrations and tumor immune microenvironment in primary acral melanoma.

Journal Of Translational Medicine
Huang, Rong R; Shen, Gaigai G; Ren, Yu Y; Zheng, Kelin K; Wang, Jiayu J; Shi, Yan Y; Yin, Jiani C JC; Qin, Lanqun L; Zhang, Guiying G; Zhao, Mengke M; Su, Xinyu X; Li, Luqiao L; Wang, Fufeng F; Shao, Yang Y; Liu, Baorui B; Zou, Zhengyun Z
Publication Date: 2023-02-04

Variant appearance in text: BRAF: T599_V600delinsRE
PubMed Link: 36739402
Variant Present in the following documents:
  • Main text
  • 12967_2022_Article_3856.pdf
View BVdb publication page



Erdheim-Chester disease associated with a novel, complex BRAF p.Thr599_Val600delinsArgGlu mutation.

Bmj Case Reports
Bentel, Jacqueline May JM; Thomas, Marc Andrew MA; Rodgers, Jamie John JJ; Arooj, Mahreen M; Gray, Elin E; Allcock, Richard R; Fermoyle, Soraya S; Mancera, Ricardo Luis RL; Cannell, Paul P; Parry, Jeremy J
Publication Date: 2017-04-28

Variant appearance in text: BRAF: Thr599_Val600delinsArgGlu
PubMed Link: 28455460
Variant Present in the following documents:
  • Main text
View BVdb publication page