rs1057519703
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The GIST of targeted therapy for malignant melanoma.
|
24531699 |
2014 |
rs1057519703
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Transcriptome sequencing of melanocytic nevi and melanomas from Grm1 transgenic mice to determine melanoma driver mutations.
|
24661573 |
2014 |
rs1057519705
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Transcriptome sequencing of melanocytic nevi and melanomas from Grm1 transgenic mice to determine melanoma driver mutations.
|
24661573 |
2014 |
rs1057519705
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
The GIST of targeted therapy for malignant melanoma.
|
24531699 |
2014 |
rs1057519706
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Transcriptome sequencing of melanocytic nevi and melanomas from Grm1 transgenic mice to determine melanoma driver mutations.
|
24661573 |
2014 |
rs1057519706
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
The GIST of targeted therapy for malignant melanoma.
|
24531699 |
2014 |
rs1057519708
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The GIST of targeted therapy for malignant melanoma.
|
24531699 |
2014 |
rs1057519708
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Transcriptome sequencing of melanocytic nevi and melanomas from Grm1 transgenic mice to determine melanoma driver mutations.
|
24661573 |
2014 |
rs121913517
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
A meta-analysis of somatic mutations from next generation sequencing of 241 melanomas: a road map for the study of genes with potential clinical relevance.
|
24755198 |
2014 |
rs121913517
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Transcriptome sequencing of melanocytic nevi and melanomas from Grm1 transgenic mice to determine melanoma driver mutations.
|
24661573 |
2014 |
rs121913517
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
rs121913517
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
The GIST of targeted therapy for malignant melanoma.
|
24531699 |
2014 |
rs121913517
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
rs121913521
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
rs121913524
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
rs121913685
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
rs1057519713
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Secondary c-Kit mutations confer acquired resistance to RTK inhibitors in c-Kit mutant melanoma cells.
|
23582185 |
2013 |
rs1057519704
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Activating c-KIT mutations in a subset of thymic carcinoma and response to different c-KIT inhibitors.
|
22357254 |
2012 |
rs121913235
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Sunitinib therapy for melanoma patients with KIT mutations.
|
22261812 |
2012 |
rs121913235
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Sunitinib therapy for melanoma patients with KIT mutations.
|
22261812 |
2012 |
rs121913514
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
[Secondary mutation of c-kit/PDGFRα genotypes after imatinib mesylate therapy and its relationship with efficacy of sunitinib].
|
22932406 |
2012 |
rs121913523
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
[Secondary mutation of c-kit/PDGFRα genotypes after imatinib mesylate therapy and its relationship with efficacy of sunitinib].
|
22932406 |
2012 |
rs121913523
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
[Secondary mutation of c-kit/PDGFRα genotypes after imatinib mesylate therapy and its relationship with efficacy of sunitinib].
|
22932406 |
2012 |
rs200375589
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
High KIT and PDGFRA are associated with shorter patients survival in gastroenteropancreatic neuroendocrine tumors, but mutations are a rare event.
|
22160160 |
2012 |
rs200375589
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
High KIT and PDGFRA are associated with shorter patients survival in gastroenteropancreatic neuroendocrine tumors, but mutations are a rare event.
|
22160160 |
2012 |