KIT c.150_151insTT ;(p.G51Lfs*54)

Variant ID: 4-55561760-G-GTT

NM_000222.2(KIT):c.150_151insTT;(p.G51Lfs*54)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of Germline Mutations in Upper Tract Urothelial Carcinoma With Suspected Lynch Syndrome.

Frontiers In Oncology
Guan, Bao B; Wang, Jie J; Li, Xuesong X; Lin, Lin L; Fang, Dong D; Kong, Wenwen W; Tian, Chuangyu C; Li, Juan J; Yang, Kunlin K; Han, Guanpeng G; Wu, Yucai Y; He, Yuhui Y; Peng, Yiji Y; Yu, Yanfei Y; He, Qun Q; He, Shiming S; Gong, Yanqing Y; Zhou, Liqun L; Tang, Qi Q
Publication Date: 2022

Variant appearance in text: KIT: 150_151insTT; Gly51fs
PubMed Link: 35372080
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
View BVdb publication page