rs28929495
|
|
|
0.720 |
GeneticVariation |
BEFREE |
Long-term survival with erlotinib in advanced lung adenocarcinoma harboring synchronous EGFR G719S and KRAS G12C mutations.
|
29748019 |
2018 |
rs28929495
|
|
|
0.720 |
GeneticVariation |
BEFREE |
We herein first report G719S mutation in lung adenocarcinoma with tonsillar metastasis.
|
29245278 |
2017 |
rs28929495
|
|
T |
0.720 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121913444
|
|
|
0.710 |
GeneticVariation |
BEFREE |
The patient was diagnosed with lung adenocarcinoma with an EGFR L861Q mutation based on cytological findings.
|
31779047 |
2020 |
rs121913444
|
|
A |
0.710 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121913428
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121913428
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121913229
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
rs139429793
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Glioma Specific Extracellular Missense Mutations in the First Cysteine Rich Region of Epidermal Growth Factor Receptor (EGFR) Initiate Ligand Independent Activation.
|
24212795 |
2011 |
rs150036236
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Clinical implications of novel activating EGFR mutations in malignant peritoneal mesothelioma.
|
20942962 |
2010 |
rs121913229
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain.
|
15737014 |
2005 |
rs1554350382
|
|
AGTC |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1057519847
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Intense expression of L858R in the MP component was suggested, and the MP+ patients harboring L858R were at comparatively higher risk of recurrence in the group with pN0M0 lung adenocarcinoma.
|
31732945 |
2020 |
rs1057519848
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Intense expression of L858R in the MP component was suggested, and the MP+ patients harboring L858R were at comparatively higher risk of recurrence in the group with pN0M0 lung adenocarcinoma.
|
31732945 |
2020 |
rs121434568
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Intense expression of L858R in the MP component was suggested, and the MP+ patients harboring L858R were at comparatively higher risk of recurrence in the group with pN0M0 lung adenocarcinoma.
|
31732945 |
2020 |
rs121434569
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Lower pre-treatment PD-L1 is associated with better ORR, PFS, and higher frequency of T790M resistance in EGFR TKI-treated lung ADC patients.
|
31760310 |
2020 |
rs1057519847
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Unusual synchronous double primary treatment-naïve lung adenocarcinoma harboring T790M and L858R mutations in early-stage lung cancer.
|
31426797 |
2019 |
rs1057519847
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Our study suggested the intratumoral heterogeneity of EGFR-activating mutations in lung adenocarcinoma confirmed on the single-cell level, which might be associated with EGFR-TKIs response in lung adenocarcinoma patients harboring the EGFR L858R mutation.
|
31014278 |
2019 |
rs1057519847
|
|
|
0.100 |
GeneticVariation |
BEFREE |
ctDNA of EGFR-TKI sensitizing mutations (mEGFR), L858R substitution and Exon 19 deletion (E19d) mutation, was evaluated using droplet digital PCR (ddPCR) in 81 patients with lung adenocarcinoma which harbored mEGFR in the corresponding tumor tissues.
|
31647198 |
2019 |
rs1057519847
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Clinicopathologic information was analyzed and EGFR mutation results were performed in initial biopsy samples.Seven patients showed transformation from ADC to SCLC, of which 6 patients were 19 del EGFR mutation, only 1 patient is L858R mutations.
|
30896637 |
2019 |
rs1057519847
|
|
|
0.100 |
GeneticVariation |
BEFREE |
<i>EGFR</i> exon 19 deletions and L858R mutation in exon 21 are the most common sensitive mutations in lung adenocarcinoma.
|
31064887 |
2019 |
rs1057519847
|
|
|
0.100 |
GeneticVariation |
BEFREE |
A 55-year-old female with EGFR mutation (L858R) was diagnosed with lung adenocarcinoma, who was responsive to first-generation EGFR-tyrosine kinase inhibitor (TKI).
|
31382924 |
2019 |
rs1057519847
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Patients with advanced lung adenocarcinoma with membranous mutant EGFR (19del or 21 L858R) showed significantly longer progression-free survival than those with cytoplasmic mutant EGFR after gefitinib treatment.
|
31228625 |
2019 |
rs1057519848
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Our study suggested the intratumoral heterogeneity of EGFR-activating mutations in lung adenocarcinoma confirmed on the single-cell level, which might be associated with EGFR-TKIs response in lung adenocarcinoma patients harboring the EGFR L858R mutation.
|
31014278 |
2019 |
rs1057519848
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Patients with advanced lung adenocarcinoma with membranous mutant EGFR (19del or 21 L858R) showed significantly longer progression-free survival than those with cytoplasmic mutant EGFR after gefitinib treatment.
|
31228625 |
2019 |