ERBB2 c.2896_2898delinsTGT ;(p.R966C)

Variant ID: 17-37882838-CGG-TGT

NM_004448.2(ERBB2):c.2896_2898delinsTGT;(p.R966C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Analysis of somatic mutations across the kinome reveals loss-of-function mutations in multiple cancer types.

Scientific Reports
Kumar, Runjun D RD; Bose, Ron R
Publication Date: 2017-07-25

Variant appearance in text: HER2: R966C
PubMed Link: 28743916
Variant Present in the following documents:
  • Main text
  • 41598_2017_6366_MOESM5_ESM.xls, sheet 3
  • 41598_2017_Article_6366.pdf
View BVdb publication page