rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
|
27153395 |
2016 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations.
|
26650189 |
2016 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup.
|
26775776 |
2016 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Characterization of patients at high risk of melanoma in Austria.
|
26800492 |
2016 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma.
|
27680874 |
2016 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genetic susceptibility to cutaneous melanoma in southern Switzerland: role of CDKN2A, MC1R and MITF.
|
27473757 |
2016 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The Microphthalmia-Associated Transcription Factor p.E318K Mutation Does Not Play a Major Role in Sporadic Renal Cell Tumors from Caucasian Patients.
|
26999813 |
2016 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition.
|
25803691 |
2015 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A germline oncogenic MITF mutation and tumor susceptibility.
|
24290354 |
2015 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The lack of E318K MITF germline mutation in Latvian melanoma patients.
|
25975176 |
2015 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genotype analysis in Hungarian patients with multiple primary melanoma.
|
24660985 |
2014 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
MITF E318K's effect on melanoma risk independent of, but modified by, other risk factors.
|
24406078 |
2014 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Phenotypic characterization of nevus and tumor patterns in MITF E318K mutation carrier melanoma patients.
|
23774529 |
2014 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of the E318K and V320I MITF germline mutations in Polish cancer patients and multiorgan cancer risk-a population-based study.
|
24767713 |
2014 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Malignant and benign tumors associated with multiple primary melanomas: just the starting block for the involvement of MITF, PTEN and CDKN2A in multiple cancerogenesis?
|
23802662 |
2013 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genetic counseling in melanoma.
|
23046018 |
2013 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
MITF mutations associated with pigment deficiency syndromes and melanoma have different effects on protein function.
|
23787126 |
2013 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history.
|
23167872 |
2013 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
|
22012259 |
2011 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
|
22080950 |
2011 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Cancer genomics: Finding a rare variant.
|
22158021 |
2011 |
rs149617956
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Conformation of cytoplasmic segments of acetylcholine receptor alpha- and beta-subunits probed by monoclonal antibodies: sensitivity of the antibody competition approach.
|
2440678 |
1987 |
rs149617956
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|