KIT c.1675_1677delinsTAA ;(p.V559*)

Variant ID: 4-55593609-GTT-TAA

NM_000222.2(KIT):c.1675_1677delinsTAA;(p.V559*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Exon 11 homozygous mutations and intron 10/exon 11 junction deletions in the KIT gene are associated with poor prognosis of patients with gastrointestinal stromal tumors.

Cancer Medicine
Shen, Yan-Ying YY; Ma, Xin-Li XL; Wang, Ming M; Zhuang, Chun C; Ni, Bo B; Tu, Lin L; Liu, Qiang Q; Zhao, Wen-Yi WY; Cao, Hui H
Publication Date: 2020-09

Variant appearance in text: KIT: V559X
PubMed Link: 32697050
Variant Present in the following documents:
  • Main text
  • CAM4-9-6485.pdf
View BVdb publication page



Targeted therapy in cancer.

Cancer Chemotherapy And Pharmacology
Tsimberidou, Apostolia-Maria AM
Publication Date: 2015-12

Variant appearance in text: KIT: V559X
PubMed Link: 26391154
Variant Present in the following documents:
  • Main text
View BVdb publication page