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ERBB2 c.2667G>A ;(p.M889I)
Variant ID: 17-37881597-G-A
NM_004448.2(
ERBB2
):c.2667G>A;(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