Bibliome.ai browser hg19
Search
About
Stats
FAQ
ERBB2 c.3139_3140delinsGC ;(p.H1047A)
Variant ID: 17-37883236-CA-GC
NM_004448.2(
ERBB2
):c.3139_3140delinsGC;(p.H1047A)
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:
Epigenetic dysregulation in meningiomas.
Neuro-Oncology Advances
Wedemeyer, Michelle A MA; Muskens, Ivo I; Strickland, Ben A BA; Aurelio, Oscar O; Martirosian, Vahan V; Wiemels, Joseph L JL; Weisenberger, Daniel J DJ; Wang, Kai K; Mukerjee, Debraj D; Rhie, Suhn K SK; Zada, Gabriel G
Publication Date: 2022
Variant appearance in text: ERBB2: H1047A
PubMed Link:
35769412
Variant Present in the following documents:
vdac084.pdf
View BVdb publication page
Disease characterization in liquid biopsy from HER2-mutated, non-amplified metastatic breast cancer patients treated with neratinib.
Npj Breast Cancer
Shishido, Stephanie N SN; Masson, Rahul R; Xu, Liya L; Welter, Lisa L; Prabakar, Rishvanth Kaliappan RK; D' Souza, Anishka A; Spicer, Darcy D; Kang, Irene I; Jayachandran, Priya P; Hicks, James J; Lu, Janice J; Kuhn, Peter P
Publication Date: 2022-02-18
Variant appearance in text: ERBB2: H1047A
PubMed Link:
35181666
Variant Present in the following documents:
41523_2022_Article_390.pdf
View BVdb publication page