Gene: BRAF ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913351
rs121913351
BRAF
A 0.700 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913351
rs121913351
BRAF
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913351
rs121913351
BRAF
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913355
rs121913355
BRAF
G 0.700 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913355
rs121913355
BRAF
T 0.700 CausalMutation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913357
rs121913357
BRAF
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913370
rs121913370
BRAF
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913370
rs121913370
BRAF
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs180177040
rs180177040
BRAF
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs397516896
rs397516896
BRAF
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs397516896
rs397516896
BRAF
T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs121913338
rs121913338
BRAF
C 0.700 CausalMutation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913361
rs121913361
BRAF
G 0.700 CausalMutation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913338
rs121913338
BRAF
C 0.700 CausalMutation CLINVAR The road to resistance: EGFR mutation and cetuximab. 22310681

2012
dbSNP: rs121913351
rs121913351
BRAF
A 0.700 CausalMutation CLINVAR The road to resistance: EGFR mutation and cetuximab. 22310681

2012
dbSNP: rs121913355
rs121913355
BRAF
A 0.700 CausalMutation CLINVAR The road to resistance: EGFR mutation and cetuximab. 22310681

2012
dbSNP: rs121913355
rs121913355
BRAF
G 0.700 CausalMutation CLINVAR The road to resistance: EGFR mutation and cetuximab. 22310681

2012
dbSNP: rs121913355
rs121913355
BRAF
T 0.700 CausalMutation CLINVAR The road to resistance: EGFR mutation and cetuximab. 22310681

2012
dbSNP: rs121913361
rs121913361
BRAF
G 0.700 CausalMutation CLINVAR The road to resistance: EGFR mutation and cetuximab. 22310681

2012
dbSNP: rs121913361
rs121913361
BRAF
G 0.700 CausalMutation CLINVAR Antitumor activity of BRAF inhibitor vemurafenib in preclinical models of BRAF-mutant colorectal cancer. 22180495

2012
dbSNP: rs727502902
rs727502902
BRAF
TGTA 0.700 CausalMutation CLINVAR Distinguishing clinicopathologic features of patients with V600E and V600K BRAF-mutant metastatic melanoma. 22535154

2012
dbSNP: rs727502902
rs727502902
BRAF
TGTA 0.700 CausalMutation CLINVAR BRAF, p53 and SOX2 in anaplastic thyroid carcinoma: evidence for multistep carcinogenesis. 21716161

2011
dbSNP: rs727502902
rs727502902
BRAF
TGTA 0.700 CausalMutation CLINVAR Prognostic and clinicopathologic associations of oncogenic BRAF in metastatic melanoma. 21343559

2011
dbSNP: rs727502902
rs727502902
BRAF
TGTA 0.700 CausalMutation CLINVAR Functional characterization of a BRAF insertion mutant associated with pilocytic astrocytoma. 21190184

2011
dbSNP: rs121913338
rs121913338
BRAF
C 0.700 CausalMutation CLINVAR Effects of KRAS, BRAF, NRAS, and PIK3CA mutations on the efficacy of cetuximab plus chemotherapy in chemotherapy-refractory metastatic colorectal cancer: a retrospective consortium analysis. 20619739

2010