KIT c.1098G>C ;(p.E366D)

Variant ID: 4-55573436-G-C

NM_000222.2(KIT):c.1098G>C;(p.E366D)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A full-proteome, interaction-specific characterization of mutational hotspots across human cancers.

Genome Research
Chen, Siwei S; Liu, Yuan Y; Zhang, Yingying Y; Wierbowski, Shayne D SD; Lipkin, Steven M SM; Wei, Xiaomu X; Yu, Haiyuan H
Publication Date: 2022-01

Variant appearance in text: KIT: E366D
PubMed Link: 34963661
Variant Present in the following documents:
  • supp_gr.275437.121_Supplementary_Table_1.xlsx, sheet 3
View BVdb publication page



Next-Generation Sequencing Whole-Genome Analysis for Targeted Treatment Approach of Metastatic Bartholin Gland Adenocarcinoma: An Emblematic Case Report and Review of the Literature.

Diagnostics (Basel, Switzerland)
Macciò, Antonio A; Donisi, Clelia C; Sanna, Elisabetta E; Chiappe, Giacomo G; Nemolato, Sonia S; Melis, Luca L; Oppi, Sara S; Mola, Brunella B; Madeddu, Clelia C
Publication Date: 2021-11-10

Variant appearance in text: KIT: E366D
PubMed Link: 34829431
Variant Present in the following documents:
  • Main text
View BVdb publication page