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ERBB2 c.52C>A ;(p.P18T)
Variant ID: 17-37856543-C-A
NM_004448.2(
ERBB2
):c.52C>A;(p.P18T)
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:
Analysis of Circulating Tumor DNA to Predict Neoadjuvant Therapy Effectiveness and Breast Cancer Recurrence.
Journal Of Breast Cancer
Hao, Shuai S; Tian, Wuguo W; Zhao, Jianjie J; Chen, Yi Y; Zhang, Xiaohua X; Gao, Bo B; He, Yujun Y; Luo, Donglin D
Publication Date: 2020-08
Variant appearance in text: ERBB2: P18T
PubMed Link:
32908788
Variant Present in the following documents:
jbc-23-373-s004.xls, sheet 1
View BVdb publication page
CRISPR-induced RASGAP deficiencies in colorectal cancer organoids reveal that only loss of NF1 promotes resistance to EGFR inhibition.
Oncotarget
Post, Jasmin B JB; Hami, Nizar N; Mertens, Alexander E E AEE; Elfrink, Suraya S; Bos, Johannes L JL; Snippert, Hugo J G HJG
Publication Date: 2019-02-15
Variant appearance in text: HER2: P18T
PubMed Link:
30858928
Variant Present in the following documents:
Main text
View BVdb publication page