Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267599211
rs267599211
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0151779
Disease:
Cutaneous Melanoma 		T 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs267599211
rs267599211
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0151779
Disease:
Cutaneous Melanoma 		0.710 GeneticVariation BEFREE Whole exome sequencing identifies a recurrent RQCD1 P131L mutation in cutaneous melanoma. 25544760 2015
dbSNP: rs1057519955
rs1057519955
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0151779
Disease:
Cutaneous Melanoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519956
rs1057519956
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C2239176
Disease:
Liver carcinoma 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519956
rs1057519956
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0279680
Disease:
Transitional cell carcinoma of bladder 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519956
rs1057519956
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0007112
Disease:
Adenocarcinoma of prostate 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519956
rs1057519956
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0151779
Disease:
Cutaneous Melanoma 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519956
rs1057519956
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519957
rs1057519957
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0007112
Disease:
Adenocarcinoma of prostate 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519957
rs1057519957
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0279680
Disease:
Transitional cell carcinoma of bladder 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519957
rs1057519957
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519957
rs1057519957
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0151779
Disease:
Cutaneous Melanoma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519957
rs1057519957
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C2239176
Disease:
Liver carcinoma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs267599211
rs267599211
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C2739810
Disease:
Lentigo maligna melanoma 		0.010 GeneticVariation BEFREE Compared to tumors without the mutation, the P131L mutant positive tumors were associated with increased thickness (p = 0.02), head and neck (p = 0.009) and upper limb (p = 0.03) location, lentigo maligna melanoma subtype (p = 0.02) and BRAF V600K (p = 0.04) but not V600E or NRAS codon 61 mutations. 25544760 2015
dbSNP: rs267599211
rs267599211
Entrez Id: 9125
Gene Symbol: CNOT9
CNOT9
CUI: C0025202
Disease:
melanoma 		0.010 GeneticVariation BEFREE Whole exome sequencing identifies a recurrent RQCD1 P131L mutation in cutaneous melanoma. 25544760 2015