KIT c.789T>G ;(p.H263Q)

Variant ID: 4-55569922-T-G

NM_000222.2(KIT):c.789T>G;(p.H263Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Development and validation of a multigene variant profiling assay to guide targeted and immuno therapy selection in solid tumors.

Plos One
Akolkar, Dadasaheb D; Patil, Darshana D; Srivastava, Navin N; Patil, Revati R; Datta, Vineet V; Apurwa, Sachin S; Yashwante, Nitin N; Dhasarathan, Raja R; Gosavi, Rahul R; John, Jinumary J; Khan, Shabishta S; Jadhav, Ninad N; Mene, Priti P; Ahire, Dhanashri D; Pawar, Sushant S; Bodke, Harshal H; Sahoo, Subhraline S; Nile, Arun A; Saindane, Dinesh D; Darokar, Harshal H; Devhare, Pradip P; Srinivasan, Ajay A; Datar, Rajan R
Publication Date: 2021

Variant appearance in text: KIT: H263Q
PubMed Link: 33556149
Variant Present in the following documents:
  • pone.0246048.s008.xlsx, sheet 1
View BVdb publication page



Targeted next generation sequencing identifies somatic mutations in a cohort of Egyptian breast cancer patients.

Journal Of Advanced Research
Nassar, Auhood A; Abouelhoda, Mohamed M; Mansour, Osman O; Loutfy, Samah A SA; Hafez, Mohamed M MM; Gomaa, M M; Bahnassy, Abeer A; El-Din Youssef, Amira Salah AS; Lotfy, Mai M MM; Ismail, Hoda H; Ahmed, Ola S OS; Abou-Bakr, Amany Abd-Elhameed AA; Zekri, Abdel-Rahman N AN
Publication Date: 2020-07

Variant appearance in text: KIT: 789T>G; H263Q
PubMed Link: 32322420
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page