Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913465
rs121913465
0.050 GeneticVariation BEFREE Effectiveness of afatinib after ineffectiveness of gefitinib in an advanced lung adenocarcinoma patient with a single EGFR exon 20 S768I mutation: a case report. 29731638

2018

dbSNP: rs121913465
rs121913465
0.050 GeneticVariation BEFREE Synchronous occurrence of squamous-cell carcinoma "transformation" and EGFR exon 20 S768I mutation as a novel mechanism of resistance in EGFR-mutated lung adenocarcinoma. 28024692

2017

dbSNP: rs121913465
rs121913465
0.050 GeneticVariation BEFREE This study aimed to investigate the prevalence of the S768I mutation in Chinese patients with lung AC and to retrospectively analyze the response of S768I mutants to tyrosine kinase inhibitors (TKIs). 27538584

2017

dbSNP: rs121913465
rs121913465
0.050 GeneticVariation BEFREE Primary lung adenocarcinoma occurring in a PTEN related syndrome (Cowden's disease): routine EGFR sequencing also highlights two rare somatic mutations S768I and V769L. 23261230

2013

dbSNP: rs121913465
rs121913465
0.050 GeneticVariation BEFREE Here, we report the first case of adenocarcinoma of the lung in which the patient had rare mutations S768I and V769L and was treated with gefitinib. 17045698

2006