ERBB2 c.2667G>C ;(p.M889I)

Variant ID: 17-37881597-G-C

NM_004448.2(ERBB2):c.2667G>C;(p.M889I)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Somatic Mutations in HER2 and Implications for Current Treatment Paradigms in HER2-Positive Breast Cancer.

Journal Of Oncology
Gaibar, Maria M; Beltrán, Laura L; Romero-Lorca, Alicia A; Fernández-Santander, Ana A; Novillo, Apolonia A
Publication Date: 2020

Variant appearance in text: HER2: M889I
PubMed Link: 32256585
Variant Present in the following documents:
  • Main text
  • JO2020-6375956.pdf
View BVdb publication page