FAT1 c.3998C>T ;(p.P1333L)

Variant ID: 4-187557364-G-A

NM_005245.3(FAT1):c.3998C>T;(p.P1333L)

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: P1333L
PubMed Link: 34963661
Variant Present in the following documents:
  • supp_gr.275437.121_Supplementary_Table_1.xlsx, sheet 3
View BVdb publication page



Unique Aberrations in Intimal Sarcoma Identified by Next-Generation Sequencing as Potential Therapy Targets.

Cancers
Roszik, Jason J; Khan, Abir A; Conley, Anthony P AP; Livingston, J Andrew JA; Groisberg, Roman R; Ravi, Vinod V; Carmagnani Pestana, Roberto R; Sen, Shiraj S; Subbiah, Vivek V
Publication Date: 2019-08-31

Variant appearance in text: FAT1: P1333L
PubMed Link: 31480474
Variant Present in the following documents:
  • Main text
View BVdb publication page