Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913465
rs121913465
0.010 GeneticVariation BEFREE We describe here on a hitherto unreported mechanism of EGFR TKI resistance synchronously combining squamous-cell carcinoma change and occurrence of the EGFR exon 20 S768I secondary mutation in a 43 year-old woman with stage IV adenocarcinoma harbouring EGFR exon 21 L858R mutation. 28024692

2017

dbSNP: rs150423237
rs150423237
0.010 GeneticVariation BEFREE An adenocarcinoma patient with JM R675Q had erlotinib, 150 mg daily, added following progression of disease on carboplatin and paclitaxel and had a partial response for 4 months. 28573640

2017

dbSNP: rs397517108
rs397517108
0.010 GeneticVariation BEFREE We describe here on a hitherto unreported mechanism of EGFR TKI resistance synchronously combining squamous-cell carcinoma change and occurrence of the EGFR exon 20 S768I secondary mutation in a 43 year-old woman with stage IV adenocarcinoma harbouring EGFR exon 21 L858R mutation. 28024692

2017

dbSNP: rs28929495
rs28929495
0.010 GeneticVariation BEFREE Seven of 17 cases (41%) were reclassified in the adenocarcinoma with solid pattern group, which showed one KRAS G12C and one EGFR E709K + G719C double mutation in addition to mutations in TP53. 26430808

2016

dbSNP: rs2227983
rs2227983
0.010 GeneticVariation BEFREE We investigated the EGFR mutations and/or R497K polymorphism statuses in 225 surgically treated NSCLC cases.192 adenocarcinoma cases were included. 18726117

2009

dbSNP: rs146795390
rs146795390
0.010 GeneticVariation BEFREE These observations suggest that the germline EGFR V843I mutation might have altered EGFR signaling in the multicentric development of adenocarcinoma, bronchoalveolar carcinoma, and atypical adenomatous hyperplasia and also might have had a role in the development of lung cancer in multiple members of her family. 18355544

2008

dbSNP: rs373129709
rs373129709
0.010 GeneticVariation BEFREE The aim of the present study was to investigate the relationship between EGF A61G genotype and EGF gene expression levels in colorectal adenocarcinomas and normal colon tissue. 17851837

2007

dbSNP: rs121913444
rs121913444
0.020 GeneticVariation BEFREE Tumor cells were separately collected from components of both the LCNEC and adenocarcinoma, and a mutational analysis of the epidermal growth factor receptor (EGFR) gene demonstrated that both components had the same L861Q mutation at exon 21. 23518631

2014

dbSNP: rs121913444
rs121913444
0.020 GeneticVariation BEFREE Seven months after initial diagnosis, the primary tumor enlarged again, and a second biopsy from the enlarged lesion detected only adenocarcinoma with the L861Q mutation. 24195468

2013

dbSNP: rs397517132
rs397517132
0.050 GeneticVariation BEFREE Lung ADCA harbouring BRAF mutations are commonly non-V600E. 30591192

2019

dbSNP: rs397517132
rs397517132
0.050 GeneticVariation BEFREE Moreover, a 47-year-old female with a recurrent adenocarcinoma and a BRAF V600E mutation exhibited tumor regression after a fourth line therapy with dabrafenib and trametinib, targeting agents against BRAF mutations. 31440061

2019

dbSNP: rs397517132
rs397517132
0.050 GeneticVariation BEFREE Twenty-one BRAF mutations were identified in 951 patients with adenocarcinomas (2.2%; 95% confidence interval [CI], 1.4%-3.4%): 17 (81%; 95% CI, 60%-92%) were BRAF(V600E) mutations, and 4 were non-BRAF(V600E) mutations. 25273224

2015

dbSNP: rs397517132
rs397517132
0.050 GeneticVariation BEFREE Adenocarcinomas with this clinicopathologic phenotype may be worthwhile investigating for BRAF-V600E mutation as more genetically oriented drug therapies emerge. 18636014

2008

dbSNP: rs397517132
rs397517132
0.050 GeneticVariation BEFREE In exon 15, one BRAF mutation (1796 thymine to adenine; V599E) was found in nonsmoking woman with well-differentiated adenocarcinoma. 16376942

2006

dbSNP: rs1057519847
rs1057519847
0.100 GeneticVariation BEFREE EGFR L858R was more frequently harbored in the MP+ adenocarcinoma patients than in the MP- adenocarcinoma patients. 31732945

2020

dbSNP: rs1057519848
rs1057519848
0.100 GeneticVariation BEFREE EGFR L858R was more frequently harbored in the MP+ adenocarcinoma patients than in the MP- adenocarcinoma patients. 31732945

2020

dbSNP: rs121434568
rs121434568
0.100 GeneticVariation BEFREE EGFR L858R was more frequently harbored in the MP+ adenocarcinoma patients than in the MP- adenocarcinoma patients. 31732945

2020

dbSNP: rs1057519847
rs1057519847
0.100 GeneticVariation BEFREE The patient was a 67-year-old male with a diagnosis of metastatic pulmonary adenocarcinoma with an L858R mutation on exon 21. 31371992

2019

dbSNP: rs1057519848
rs1057519848
0.100 GeneticVariation BEFREE The patient was a 67-year-old male with a diagnosis of metastatic pulmonary adenocarcinoma with an L858R mutation on exon 21. 31371992

2019

dbSNP: rs121434568
rs121434568
0.100 GeneticVariation BEFREE The patient was a 67-year-old male with a diagnosis of metastatic pulmonary adenocarcinoma with an L858R mutation on exon 21. 31371992

2019

dbSNP: rs121434569
rs121434569
0.100 GeneticVariation BEFREE After 12 mo of treatment with icotinib, ovarian biopsy showed adenocarcinoma with CDX2(-), TTF-1(+++), PAX8(-), CK-7(+++), CK-20(++), and Ki67(15%+), accompanied with EGFR 19-del mutation and T790M mutation. 31363481

2019

dbSNP: rs121434569
rs121434569
0.100 GeneticVariation BEFREE We studied the prevalence of T790M mutation among pulmonary adenocarcinoma patients in Lebanese patients based on liquid biopsy testing the circulating tumor DNA (ctDNA). 31147859

2019

dbSNP: rs1057519847
rs1057519847
0.100 GeneticVariation BEFREE Inclusion criteria were histologic diagnosis of benign nodule (control) and stage I or II adenocarcinoma harboring either p.L858R or ex</span>on19 delEGFR mutations. 30309763

2018

dbSNP: rs1057519847
rs1057519847
0.100 GeneticVariation BEFREE This case represents the first evidence that 1) bevacizumab combined with osimertinib can significantly relieve tumor growth and respiratory symptoms in non-small-cell lung cancer patients with osimertinib resistance and 2) the clinical use of osimertinib, bevacizumab, and brigatinib is effective as combination therapy for pulmonary adenocarcinoma in the presence of triple EGFR mutations of L858R, T790M, and <i>cis</i>-C797S. 30233215

2018

dbSNP: rs1057519847
rs1057519847
0.100 GeneticVariation BEFREE A 62-year-old Asian male never smoker who presented with stage IV EGFR L858R-positive adenocarcinoma developed EGFR T790 M mutation after 14 months of treatment with erlotinib combined with thoracic radiotherapy as first-line therapy. 30400855

2018