Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
G 0.800 CausalMutation CLINVAR N-ras mutations in human cutaneous melanoma from sun-exposed body sites. 2674680

1989

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
C 0.800 CausalMutation CLINVAR N-ras mutations in human cutaneous melanoma from sun-exposed body sites. 2674680

1989

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
A 0.800 CausalMutation CLINVAR N-ras mutations in human cutaneous melanoma from sun-exposed body sites. 2674680

1989

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
A 0.800 CausalMutation CLINVAR Ras mutations in human melanoma: a marker of malignant progression. 8120410

1994

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
G 0.800 CausalMutation CLINVAR Ras mutations in human melanoma: a marker of malignant progression. 8120410

1994

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
C 0.800 CausalMutation CLINVAR Ras mutations in human melanoma: a marker of malignant progression. 8120410

1994

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
0.800 GeneticVariation BEFREE We studied global gene expression in three melanoma cell lines with the most common and potent V600E mutation in the B-RAF gene-four cell lines with a common Q61R mutation in the N-RAS gene and three cell lines with no mutations using human HG-U133A 2.0 micro-arrays with 22 277 transcripts. 15760917

2005

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
C 0.800 CausalMutation CLINVAR Distinct sets of genetic alterations in melanoma. 16291983

2005

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
G 0.800 CausalMutation CLINVAR Distinct sets of genetic alterations in melanoma. 16291983

2005

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
A 0.800 CausalMutation CLINVAR Distinct sets of genetic alterations in melanoma. 16291983

2005

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
A 0.800 CausalMutation CLINVAR Phase I pharmacokinetic and pharmacodynamic study of the oral, small-molecule mitogen-activated protein kinase kinase 1/2 inhibitor AZD6244 (ARRY-142886) in patients with advanced cancers. 18390968

2008

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
G 0.800 CausalMutation CLINVAR Phase I pharmacokinetic and pharmacodynamic study of the oral, small-molecule mitogen-activated protein kinase kinase 1/2 inhibitor AZD6244 (ARRY-142886) in patients with advanced cancers. 18390968

2008

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
C 0.800 CausalMutation CLINVAR Phase I pharmacokinetic and pharmacodynamic study of the oral, small-molecule mitogen-activated protein kinase kinase 1/2 inhibitor AZD6244 (ARRY-142886) in patients with advanced cancers. 18390968

2008

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
0.800 GeneticVariation BEFREE Reciprocally, overexpression of C-MYC in normal melanocytes suppressed BRAF(V600E)-induced senescence more efficiently than NRAS(Q61R)-induced senescence, which agrees with the generally higher rates of activating mutations in BRAF than NRAS gene in human cutaneous me</span>lanomas. 18679422

2008

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
G 0.800 CausalMutation CLINVAR RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth. 20130576

2010

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
C 0.800 CausalMutation CLINVAR RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth. 20130576

2010

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
A 0.800 CausalMutation CLINVAR RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth. 20130576

2010

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
A 0.800 CausalMutation CLINVAR Furthermore, PLX4032 increased the rate of proliferation of growth factor-dependent NRAS Q61L mutant primary melanoma cells, reduced cell adherence and increased mobility of cells from advanced lesions. 20149136

2010

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
A 0.800 CausalMutation CLINVAR RAF inhibitors transactivate RAF dimers and ERK signalling in cells with wild-type BRAF. 20179705

2010

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
C 0.800 CausalMutation CLINVAR RAF inhibitors transactivate RAF dimers and ERK signalling in cells with wild-type BRAF. 20179705

2010

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
G 0.800 CausalMutation CLINVAR RAF inhibitors transactivate RAF dimers and ERK signalling in cells with wild-type BRAF. 20179705

2010

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
A 0.800 CausalMutation CLINVAR Differential sensitivity of melanoma cell lines with BRAFV600E mutation to the specific Raf inhibitor PLX4032. 20406486

2010

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
0.800 GeneticVariation BEFREE We have evaluated five real-time ARMS assays: BRAF 1799T>A, [this includes V600E and V600K] and NRAS 182A>G [Q61R] and 181C>A [Q61K] in melanoma, EGFR 2573T>G [L858R], 2235-2249del15 [E746-A750del] in non-small-cell lung cancer, and compared the results to DNA sequencing of the mutation 'hot-spots' in these genes in formalin-fixed paraffin-embedded tumour (FF-PET) DNA. 20925915

2010

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
C 0.800 CausalMutation CLINVAR Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation. 21107323

2010

dbSNP: rs11554290
rs11554290
CUI: C0025202
Disease: melanoma
melanoma
A 0.800 CausalMutation CLINVAR NRAS-mutant melanoma: response to chemotherapy. 21576590

2011