ERBB2 c.2576T>A ;(p.V859D)

Variant ID: 17-37881384-T-A

NM_004448.2(ERBB2):c.2576T>A;(p.V859D)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Landscape of Genomic Alterations and PD-L1 Expression in Early-Stage Non-Small-Cell Lung Cancer (NSCLC)-A Single Center, Retrospective Observational Study.

International Journal Of Molecular Sciences
Stephan-Falkenau, Susann S; Streubel, Anna A; Mairinger, Thomas T; Kollmeier, Jens J; Misch, Daniel D; Thiel, Sebastian S; Bauer, Torsten T; Pfannschmidt, Joachim J; Hollmann, Manuel M; Wessolly, Michael M; Blum, Torsten Gerriet TG
Publication Date: 2022-10-19

Variant appearance in text: ERBB2: V859D
PubMed Link: 36293366
Variant Present in the following documents:
  • Main text
  • ijms-23-12511.pdf
View BVdb publication page



Application of a multi-gene next-generation sequencing panel to a non-invasive oesophageal cell-sampling device to diagnose dysplastic Barrett's oesophagus.

The Journal Of Pathology. Clinical Research
Katz-Summercorn, Annalise A; Anand, Shubha S; Ingledew, Sophie S; Huang, Yuanxue Y; Roberts, Thomas T; Galeano-Dalmau, Nuria N; O'Donovan, Maria M; Liu, Hongxiang H; Fitzgerald, Rebecca C RC
Publication Date: 2017-10

Variant appearance in text: ERBB2: 2576T>A
PubMed Link: 29085666
Variant Present in the following documents:
  • CJP2-3-258-s005.xlsx, sheet 1
View BVdb publication page



False positives in multiplex PCR-based next-generation sequencing have unique signatures.

The Journal Of Molecular Diagnostics : Jmd
McCall, Chad M CM; Mosier, Stacy S; Thiess, Michele M; Debeljak, Marija M; Pallavajjala, Aparna A; Beierl, Katie K; Deak, Kristen L KL; Datto, Michael B MB; Gocke, Christopher D CD; Lin, Ming-Tseh MT; Eshleman, James R JR
Publication Date: 2014-09

Variant appearance in text: ERBB2: V859D
PubMed Link: 25017478
Variant Present in the following documents:
  • Main text
View BVdb publication page