KMT2C c.4549G>T ;(p.G1517*)

Variant ID: 7-151891205-C-A

NM_170606.2(KMT2C):c.4549G>T;(p.G1517*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Identification of relevant genetic alterations in cancer using topological data analysis.

Nature Communications
Rabadán, Raúl R; Mohamedi, Yamina Y; Rubin, Udi U; Chu, Tim T; Alghalith, Adam N AN; Elliott, Oliver O; Arnés, Luis L; Cal, Santiago S; Obaya, Álvaro J ÁJ; Levine, Arnold J AJ; Cámara, Pablo G PG
Publication Date: 2020-07-30

Variant appearance in text: KMT2C: G1517*
PubMed Link: 32732999
Variant Present in the following documents:
  • 41467_2020_17659_MOESM3_ESM.xls, sheet 1
View BVdb publication page



Insights into the genomic landscape of MYD88 wild-type Waldenström macroglobulinemia.

Blood Advances
Hunter, Zachary R ZR; Xu, Lian L; Tsakmaklis, Nickolas N; Demos, Maria G MG; Kofides, Amanda A; Jimenez, Cristina C; Chan, Gloria G GG; Chen, Jiaji J; Liu, Xia X; Munshi, Manit M; Gustine, Joshua J; Meid, Kirsten K; Patterson, Christopher J CJ; Yang, Guang G; Dubeau, Toni T; Samur, Mehmet K MK; Castillo, Jorge J JJ; Anderson, Kenneth C KC; Munshi, Nikhil C NC; Treon, Steven P SP
Publication Date: 2018-11-13

Variant appearance in text: KMT2C: G1517*
PubMed Link: 30401751
Variant Present in the following documents:
  • Main text
View BVdb publication page