KIT c.1744_1745inv ;(p.W582Q)

Variant ID: 4-55593678-TG-CA

NM_000222.2(KIT):c.1744_1745inv;(p.W582Q)

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: W582Q
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Screening of C-kit gene Mutation in Acute Myeloid Leukaemia in Northern India.

Iranian Journal Of Cancer Prevention
Hussain, S R SR; Raza, S T ST; Babu, S G SG; Singh, P P; Naqvi, H H; Mahdi, F F
Publication Date: 2012

Variant appearance in text: KIT: Trp582Gln
PubMed Link: 25780536
Variant Present in the following documents:
  • Main text
  • IJCP-05-027.pdf
View BVdb publication page