NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 611; N. variants: 17
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519695
rs1057519695
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0023449
Disease:
Acute lymphocytic leukemia
0.010 GeneticVariation BEFREE Early T-Cell Precursor Acute Lymphoblastic Leukemia in an Infant With an NRAS Q61R Mutation and Clinical Features of Juvenile Myelomonocytic Leukemia. 27145535 2016
dbSNP: rs1057519834
rs1057519834
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0023449
Disease:
Acute lymphocytic leukemia
0.010 GeneticVariation BEFREE Early T-Cell Precursor Acute Lymphoblastic Leukemia in an Infant With an NRAS Q61R Mutation and Clinical Features of Juvenile Myelomonocytic Leukemia. 27145535 2016
dbSNP: rs11554290
rs11554290
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0023449
Disease:
Acute lymphocytic leukemia
0.010 GeneticVariation BEFREE Early T-Cell Precursor Acute Lymphoblastic Leukemia in an Infant With an NRAS Q61R Mutation and Clinical Features of Juvenile Myelomonocytic Leukemia. 27145535 2016
dbSNP: rs121913237
rs121913237
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0280141
Disease:
Acute Undifferentiated Leukemia
0.010 GeneticVariation BEFREE Analysis of the gene-expression patterns of leukemic subpopulations revealed that the NRAS(G12V)-mediated leukemia self-renewal signature is preferentially expressed in the leukemia stem cell-enriched subpopulation. 25316678 2014
dbSNP: rs121913237
rs121913237
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0001418
Disease:
Adenocarcinoma
0.010 GeneticVariation BEFREE In all components (bilateral serous borderline tumors, low-grade serous carcinoma and mesonephric-like adenocarcinoma), an identical KRAS mutation was detected (NM_004985.4): c.35G>A, p.(G12D) proving a clonal association between the serous and mesonephric-like components and excluding a collision neoplasm. 30575604 2020
dbSNP: rs11554290
rs11554290
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder)
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs11554290
rs11554290
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder)
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs11554290
rs11554290
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder)
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs121913255
rs121913255
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder)
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs121913237
rs121913237
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0334279
Disease:
Adenocarcinoma, intestinal type
0.010 GeneticVariation BEFREE The genetic analysis showed that only 1 sinonasal ITAC (1/7) showed KRAS c.35G>C, p.(Gly12Ala) mutation, whereas BRAF and NRAS genes were wild type. 27258560 2018
dbSNP: rs11554290
rs11554290
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0206686
Disease:
Adrenocortical carcinoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs11554290
rs11554290
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0206686
Disease:
Adrenocortical carcinoma
C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs11554290
rs11554290
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0206686
Disease:
Adrenocortical carcinoma
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs121913255
rs121913255
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0206686
Disease:
Adrenocortical carcinoma
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519695
rs1057519695
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C1332201
Disease:
Adult Diffuse Large B-Cell Lymphoma
0.010 GeneticVariation BEFREE Altogether, one diffuse large B-cell lymphoma and one B-cell chronic lymphocytic leukemia (B-CLL) harbored a mutation (G12S and G12A, respectively) in the K-ras gene, and one B-CLL harbored a mutation (Q61R) in the N-ras gene. 9139869 1997
dbSNP: rs1057519834
rs1057519834
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C1332201
Disease:
Adult Diffuse Large B-Cell Lymphoma
0.010 GeneticVariation BEFREE Altogether, one diffuse large B-cell lymphoma and one B-cell chronic lymphocytic leukemia (B-CLL) harbored a mutation (G12S and G12A, respectively) in the K-ras gene, and one B-CLL harbored a mutation (Q61R) in the N-ras gene. 9139869 1997
dbSNP: rs11554290
rs11554290
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C1332201
Disease:
Adult Diffuse Large B-Cell Lymphoma
0.010 GeneticVariation BEFREE Altogether, one diffuse large B-cell lymphoma and one B-cell chronic lymphocytic leukemia (B-CLL) harbored a mutation (G12S and G12A, respectively) in the K-ras gene, and one B-CLL harbored a mutation (Q61R) in the N-ras gene. 9139869 1997
dbSNP: rs121913237
rs121913237
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C1332201
Disease:
Adult Diffuse Large B-Cell Lymphoma
0.010 GeneticVariation BEFREE Altogether, one diffuse large B-cell lymphoma and one B-cell chronic lymphocytic leukemia (B-CLL) harbored a mutation (G12S and G12A, respectively) in the K-ras gene, and one B-CLL harbored a mutation (Q61R) in the N-ras gene. 9139869 1997
dbSNP: rs121913250
rs121913250
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C1332201
Disease:
Adult Diffuse Large B-Cell Lymphoma
0.010 GeneticVariation BEFREE Altogether, one diffuse large B-cell lymphoma and one B-cell chronic lymphocytic leukemia (B-CLL) harbored a mutation (G12S and G12A, respectively) in the K-ras gene, and one B-CLL harbored a mutation (Q61R) in the N-ras gene. 9139869 1997
dbSNP: rs121913254
rs121913254
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C1332201
Disease:
Adult Diffuse Large B-Cell Lymphoma
0.010 GeneticVariation BEFREE Mutations of the BRAF gene were identified in six (24%) diffuse large B-cell lymphomas (D594G in three germinal center diffuse large B-cell lymphomas, K601N in two germinal center diffuse large B-cell lymphomas, and V600E in one non-germinal center diffuse large B-cell lymphoma) and of the NRAS gene in two (8%) non-germinal center diffuse large B-cell lymphomas (Q61K and Q61H). 22575864 2012
dbSNP: rs121913255
rs121913255
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C1332201
Disease:
Adult Diffuse Large B-Cell Lymphoma
0.010 GeneticVariation BEFREE Mutations of the BRAF gene were identified in six (24%) diffuse large B-cell lymphomas (D594G in three germinal center diffuse large B-cell lymphomas, K601N in two germinal center diffuse large B-cell lymphomas, and V600E in one non-germinal center diffuse large B-cell lymphoma) and of the NRAS gene in two (8%) non-germinal center diffuse large B-cell lymphomas (Q61K and Q61H). 22575864 2012
dbSNP: rs121913237
rs121913237
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C1332206
Disease:
Adult Lymphoma
0.010 GeneticVariation BEFREE Using a bone marrow transplant model, we previously showed that ∼ 95% of animals receiving Nras G12D/+ bone marrow cells develop chronic myelomonocytic leukemia (CMML), while ∼ 8% of recipients develop acute T-cell lymphoblastic leukemia/lymphoma [TALL] (TALL-het). 21586752 2011
dbSNP: rs121913237
rs121913237
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
CUI: C0280781
Disease:
Adult Pilocytic Astrocytoma
0.010 GeneticVariation BEFREE We screened 25 WHO I and II astrocytomas for mutations of PTPN11, NRAS, KRAS, and HRAS genes and identified the somatic G12A KRAS mutation in one pilocytic astrocytoma. 17712732 2007
dbSNP: rs8453
rs8453
Entrez Id: 4893;7812
Gene Symbol: NRAS;CSDE1
NRAS;CSDE1
CUI: C0004352
Disease:
Autistic Disorder
G 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344 2014
dbSNP: rs8453
rs8453
Entrez Id: 4893;7812
Gene Symbol: NRAS;CSDE1
NRAS;CSDE1
CUI: C0004352
Disease:
Autistic Disorder
G 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344 2014