ERBB2 c.1003_1004delinsCC ;(p.S335P)

Variant ID: 17-37868282-AG-CC

NM_004448.2(ERBB2):c.1003_1004delinsCC;(p.S335P)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


RNA-Based Multiplexing Assay for Routine Testing of Fusion and Splicing Variants in Cytological Samples of NSCLC Patients.

Diagnostics (Basel, Switzerland)
Aguado, Cristina C; Giménez-Capitán, Ana A; Román, Ruth R; Rodríguez, Sonia S; Jordana-Ariza, Núria N; Aguilar, Andrés A; Cabrera-Gálvez, Carlos C; Rivas-Corredor, Carlos C; Lianes, Pilar P; Viteri, Santiago S; Moya, Irene I; Molina-Vila, Miguel A MA
Publication Date: 2020-12-23

Variant appearance in text: ERBB2: S335P
PubMed Link: 33374879
Variant Present in the following documents:
  • Main text
  • diagnostics-11-00015.pdf
View BVdb publication page