×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Genotype-specific progression of hereditary medullary thyroid cancer.
29656518 2018
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families.
28099363 2017
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Distribution of RET Mutations in Multiple Endocrine Neoplasia 2 in Denmark 1994-2014: A Nationwide Study.
27809725 2017
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB , and SDHD Genes: Thai Experience.
28469506 2017
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
How to Assess the Clinical Relevance of Novel RET Missense Variants in the Absence of Functional Studies?
27099842 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
27539324 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Medullary Thyroid Carcinoma Associated with Germline RETK666N Mutation.
27673361 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Disease-modifying polymorphisms and C609Y mutation of RET associated with high penetrance of phaeochromocytoma and low rate of MTC in MEN2A.
27994876 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel.
26687385 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
25637381 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Molecular diagnosis and comprehensive treatment of multiple endocrine neoplasia type 2 in Southeastern Chinese.
25628771 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Skewed mutational spectrum of RET proto-oncogene Exon10 in Iranian patients with medullary thyroid carcinoma.
25694125 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma.
25810047 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
RET Cys634Arg mutation confers a more aggressive multiple endocrine neoplasia type 2A phenotype than Cys634Tyr mutation.
25515555 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
A NOVEL DOUBLE MUTATION VAL648ILE AND VAL804LEU OF RET PROTO-ONCOGENE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE 2.
26247112 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.
26269449 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Characterization of V804M-mutated RET proto-oncogene associated with familial medullary thyroid cancer, report of the largest Turkish family.
25501606 2015
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
RET revisited: expanding the oncogenic portfolio.
24561444 2014
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
A newly identified missense mutation in RET codon 666 is associated with the development of medullary thyroid carcinoma.
25319874 2014
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Patient affected by neurofibromatosis type 1 and thyroid C-cell hyperplasia harboring pathogenic germ-line mutations in both NF1 and RET genes.
24361808 2014
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
The rare intracellular RET mutation p.S891A in a Chinese Han family with familial medullary thyroid carcinoma.
24845513 2014
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
In silico profiling and structural insights of missense mutations in RET protein kinase domain by molecular dynamics and docking approach.
24336963 2014
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Multiple endocrine neoplasia type 2A in an Iranian family: clinical and genetic studies.
24784869 2014
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
The clinical spectrum of RET proto-oncogene mutations in codon 790.
23756355 2013
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Novel tandem germline RET proto-oncogene mutations in a patient with multiple endocrine neoplasia type 2B: report of a case and a literature review of tandem RET mutations with in silico analysis.
23468374 2013