RET c.1787C>T ;(p.P596L)

Variant ID: 10-43609031-C-T

NM_020975.4(RET):c.1787C>T;(p.P596L)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


NGS based identification of mutational hotspots for targeted therapy in anaplastic thyroid carcinoma.

Oncotarget
Tiedje, Vera V; Ting, Saskia S; Herold, Thomas T; Synoracki, Sarah S; Latteyer, Soeren S; Moeller, Lars C LC; Zwanziger, Denise D; Stuschke, Martin M; Fuehrer, Dagmar D; Schmid, Kurt Werner KW
Publication Date: 2017-06-27

Variant appearance in text: RET: P596L
PubMed Link: 28489587
Variant Present in the following documents:
  • Main text
  • oncotarget-08-42613.pdf
View BVdb publication page



NF1-mutated melanoma tumors harbor distinct clinical and biological characteristics.

Molecular Oncology
Cirenajwis, Helena H; Lauss, Martin M; Ekedahl, Henrik H; Törngren, Therese T; Kvist, Anders A; Saal, Lao H LH; Olsson, Håkan H; Staaf, Johan J; Carneiro, Ana A; Ingvar, Christian C; Harbst, Katja K; Hayward, Nicholas K NK; Jönsson, Göran G
Publication Date: 2017-04

Variant appearance in text: RET: 1787C>T
PubMed Link: 28267273
Variant Present in the following documents:
  • MOL2-11-438-s003.xls, sheet 1
View BVdb publication page