ERBB2 c.1696G>C ;(p.E566Q)

Variant ID: 17-37872817-G-C

NM_004448.2(ERBB2):c.1696G>C;(p.E566Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.

Plos One
Sebate, Boiketlo B; Cuttler, Katelyn K; Cloete, Ruben R; Britz, Marcell M; Christoffels, Alan A; Williams, Monique M; Carr, Jonathan J; Bardien, Soraya S
Publication Date: 2021

Variant appearance in text: ERBB2: 1696G>C; A566P
PubMed Link: 33770142
Variant Present in the following documents:
  • pone.0249324.s003.xlsx, sheet 3
View BVdb publication page



Molecular Landscape of ERBB2/ERBB3 Mutated Colorectal Cancer.

Journal Of The National Cancer Institute
Loree, Jonathan M JM; Bailey, Ann M AM; Johnson, Amber M AM; Yu, Yao Y; Wu, Wenhui W; Bristow, Christopher A CA; Davis, Jennifer S JS; Shaw, Kenna R KR; Broaddus, Russell R; Banks, Kimberly C KC; Lanman, Richard B RB; Meric-Bernstam, Funda F; Overman, Michael J MJ; Kopetz, Scott S; Raghav, Kanwal K
Publication Date: 2018-12-01

Variant appearance in text: ERBB2: E566Q
PubMed Link: 29718453
Variant Present in the following documents:
  • Main text
View BVdb publication page