KIT c.1855A>G ;(p.T619A)

Variant ID: 4-55594069-A-G

NM_000222.2(KIT):c.1855A>G;(p.T619A)

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: T619A
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Novel KIT Missense Mutation P665S in a Chinese Piebaldism Family.

Annals Of Dermatology
Zheng, Yan Y; Liu, Fen F; Yang, Yao Y; Liang, Yanhua Y
Publication Date: 2017-12

Variant appearance in text: KIT: T619A
PubMed Link: 29200776
Variant Present in the following documents:
  • Main text
  • ad-29-801.pdf
View BVdb publication page