FAT1 c.1686G>C ;(p.L562F)

Variant ID: 4-187629296-C-G

NM_005245.3(FAT1):c.1686G>C;(p.L562F)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A full-proteome, interaction-specific characterization of mutational hotspots across human cancers.

Genome Research
Chen, Siwei S; Liu, Yuan Y; Zhang, Yingying Y; Wierbowski, Shayne D SD; Lipkin, Steven M SM; Wei, Xiaomu X; Yu, Haiyuan H
Publication Date: 2022-01

Variant appearance in text: FAT1: L562F
PubMed Link: 34963661
Variant Present in the following documents:
  • supp_gr.275437.121_Supplementary_Table_1.xlsx, sheet 3
View BVdb publication page



Prognostic Significance of Oxidation Pathway Mutations in Recurrent Laryngeal Squamous Cell Carcinoma.

Cancers
Heft Neal, Molly E ME; Bhangale, Apurva D AD; Birkeland, Andrew C AC; McHugh, Jonathan B JB; Shuman, Andrew G AG; Rosko, Andrew J AJ; Swiecicki, Paul L PL; Spector, Matthew E ME; Brenner, J Chad JC
Publication Date: 2020-10-22

Variant appearance in text: FAT1: L562F
PubMed Link: 33105726
Variant Present in the following documents:
  • cancers-12-03081.pdf
View BVdb publication page