FAT1 c.3296G>A ;(p.R1099H)

Variant ID: 4-187584737-C-T

NM_005245.3(FAT1):c.3296G>A;(p.R1099H)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Clinical and genomic features of Chinese lung cancer patients with germline mutations.

Nature Communications
Peng, Wenying W; Li, Bin B; Li, Jin J; Chang, Lianpeng L; Bai, Jing J; Yi, Yuting Y; Chen, Rongrong R; Zhang, Yanyan Y; Chen, Chen C; Pu, Xingxiang X; Jiang, Meilin M; Li, Jia J; Zhong, Rui R; Xu, Fang F; Chen, Bolin B; Xu, Li L; Wang, Ning N; Huan, Jiaojiao J; Dai, Pingping P; Guan, Yanfang Y; Yang, Ling L; Xia, Xuefeng X; Yi, Xin X; Wang, Jiayin J; Yu, Fenglei F; Wu, Lin L
Publication Date: 2022-03-10

Variant appearance in text: FAT1: 3296G>A; R1099H
PubMed Link: 35273153
Variant Present in the following documents:
  • 41467_2022_28840_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page



Endometrioid endometrial cancer "recurring" as high-grade serous adenocarcinoma in the inguinal lymph nodes in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence?

Hereditary Cancer In Clinical Practice
Jiang, Wei W; Gao, Tong T; Tao, Xiang X; Zhu, Menghan M; Yao, Liangqing L; Feng, Weiwei W
Publication Date: 2019

Variant appearance in text: FAT1: R1099H; rs766055196
PubMed Link: 31139268
Variant Present in the following documents:
  • 13053_2019_112_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page