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ERBB2 c.796C>A ;(p.L266M)
Variant ID: 17-37866629-C-A
NM_004448.2(
ERBB2
):c.796C>A;(p.L266M)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Next-Generation Sequencing Reveals a Very Low Prevalence of Deleterious Mutations of Homologous Recombination Repair Genes and Homologous Recombination Deficiency in Ovarian Clear Cell Carcinoma.
Frontiers In Oncology
Liu, Hangqi H; Zhang, Zhiwen Z; Chen, Longyun L; Pang, Junyi J; Wu, Huanwen H; Liang, Zhiyong Z
Publication Date: 2021
Variant appearance in text: ERBB2: 796C>A; Leu266Met
PubMed Link:
35096598
Variant Present in the following documents:
Table_2.xlsx, sheet 1
View BVdb publication page
Mechanisms of drug resistance in kinases.
Expert Opinion On Investigational Drugs
Barouch-Bentov, Rina R; Sauer, Karsten K
Publication Date: 2011-02
Variant appearance in text: ERBB2: L266M
PubMed Link:
21235428
Variant Present in the following documents:
Main text
View BVdb publication page