KIT c.1513_1514delinsGT ;(p.N505V)

Variant ID: 4-55592189-AA-GT

NM_000222.2(KIT):c.1513_1514delinsGT;(p.N505V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Lack of SF3B1 R625 mutations in cutaneous melanoma.

Diagnostic Pathology
Schilling, Bastian B; Bielefeld, Nicola N; Sucker, Antje A; Hillen, Uwe U; Zimmer, Lisa L; Schadendorf, Dirk D; Zeschnigk, Michael M; Griewank, Klaus G KG
Publication Date: 2013-05-21

Variant appearance in text: KIT: N505V
PubMed Link: 23694694
Variant Present in the following documents:
  • Main text
  • 1746-1596-8-87.pdf
View BVdb publication page