ERBB2 c.2653C>T ;(p.P885S)

Variant ID: 17-37881583-C-T

NM_004448.2(ERBB2):c.2653C>T;(p.P885S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Finding driver mutations in cancer: Elucidating the role of background mutational processes.

Plos Computational Biology
Brown, Anna-Leigh AL; Li, Minghui M; Goncearenco, Alexander A; Panchenko, Anna R AR
Publication Date: 2019-04

Variant appearance in text: ERBB2: P885S
PubMed Link: 31034466
Variant Present in the following documents:
  • pcbi.1006981.s010.xlsx, sheet 1
View BVdb publication page



HER2 somatic mutations are associated with poor survival in HER2-negative breast cancers.

Cancer Science
Wang, Tonghui T; Xu, Ye Y; Sheng, Shuyan S; Yuan, Hua H; Ouyang, Tao T; Li, Jinfeng J; Wang, Tianfeng T; Fan, Zhaoqing Z; Fan, Tie T; Lin, Benyao B; Xie, Yuntao Y
Publication Date: 2017-04

Variant appearance in text: HER2: P885S
PubMed Link: 28164408
Variant Present in the following documents:
  • Main text
  • CAS-108-671.pdf
View BVdb publication page