Variant Gene Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434592
rs121434592
0.700 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs121434592
rs121434592
0.700 CausalMutation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2015

dbSNP: rs121434592
rs121434592
0.700 CausalMutation CLINVAR Alterations in the EGFR pathway coincide in colorectal cancer and impact on prognosis. 23934607

2013

dbSNP: rs121434592
rs121434592
0.700 CausalMutation CLINVAR Targeted sequencing of cancer-related genes in colorectal cancer using next-generation sequencing. 23700467

2013

dbSNP: rs121434592
rs121434592
0.700 CausalMutation CLINVAR A rapid, sensitive, reproducible and cost-effective method for mutation profiling of colon cancer and metastatic lymph nodes. 20233444

2010

dbSNP: rs121434592
rs121434592
0.700 CausalMutation CLINVAR A transforming mutation in the pleckstrin homology domain of AKT1 in cancer. 17611497

2007