ERBB2 c.2029_2031delinsTGG ;(p.R677W)

Variant ID: 17-37879654-CGA-TGG

NM_004448.2(ERBB2):c.2029_2031delinsTGG;(p.R677W)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.

Scientific Reports
Fransson, Susanne S; Martinez-Monleon, Angela A; Johansson, Mathias M; Sjöberg, Rose-Marie RM; Björklund, Caroline C; Ljungman, Gustaf G; Ek, Torben T; Kogner, Per P; Martinsson, Tommy T
Publication Date: 2020-12-31

Variant appearance in text: ERBB2: R677W
PubMed Link: 33384420
Variant Present in the following documents:
  • 41598_2020_Article_78370.pdf
View BVdb publication page



DiMeX: A Text Mining System for Mutation-Disease Association Extraction.

Plos One
Mahmood, A S M Ashique AS; Wu, Tsung-Jung TJ; Mazumder, Raja R; Vijay-Shanker, K K
Publication Date: 2016

Variant appearance in text: HER2: Arg677Trp
PubMed Link: 27073839
Variant Present in the following documents:
  • pone.0152725.s003.xlsx, sheet 1
View BVdb publication page