KIT c.2008A>C ;(p.T670P)

Variant ID: 4-55595518-A-C

NM_000222.2(KIT):c.2008A>C;(p.T670P)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: KIT: T670P
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Targeted therapies: the rare cancer paradigm.

Molecular Oncology
Pierotti, Marco A MA; Negri, Tiziana T; Tamborini, Elena E; Perrone, Federica F; Pricl, Sabrina S; Pilotti, Silvana S
Publication Date: 2010-02

Variant appearance in text: KIT: Thr670Pro
PubMed Link: 19913465
Variant Present in the following documents:
  • Main text
View BVdb publication page