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ERBB2 c.166G>T ;(p.V56L)
Variant ID: 17-37863335-G-T
NM_004448.2(
ERBB2
):c.166G>T;(p.V56L)
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:
Combined p53- and PTEN-deficiency activates expression of mesenchyme homeobox 1 (MEOX1) required for growth of triple-negative breast cancer.
The Journal Of Biological Chemistry
Gasparyan, Mari M; Lo, Miao-Chia MC; Jiang, Hui H; Lin, Chang-Ching CC; Sun, Duxin D
Publication Date: 2020-08-21
Variant appearance in text: HER2: 166G>T
PubMed Link:
32467227
Variant Present in the following documents:
Main text
View BVdb publication page