rs79658334
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs75076352
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC.
|
7907913 |
1994 |
rs75996173
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.
|
7881414 |
1994 |
rs76262710
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
RET proto-oncogene mutations in French MEN 2A and FMTC families.
|
7874109 |
1994 |
rs76262710
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer.
|
7849720 |
1994 |
rs77316810
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
RET proto-oncogene mutations in French MEN 2A and FMTC families.
|
7874109 |
1994 |
rs77939446
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
RET proto-oncogene mutations in inherited and sporadic medullary thyroid cancer.
|
7849720 |
1994 |
rs377767406
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects.
|
7608256 |
1995 |
rs75076352
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Activation of RET as a dominant transforming gene by germline mutations of MEN2A and MEN2B.
|
7824936 |
1995 |
rs79658334
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
RET mutations in exons 13 and 14 of FMTC patients.
|
7784092 |
1995 |
rs377767397
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A.
|
8557249 |
1996 |
rs75076352
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.
|
8918855 |
1996 |
rs77316810
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.
|
8918855 |
1996 |
rs79781594
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.
|
8918855 |
1996 |
rs79781594
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Diagnosis of multiple endocrine neoplasia [MEN] 2A, 2B and familial medullary thyroid cancer [FMTC] by multiplex PCR and heteroduplex analyses of RET proto-oncogene mutations.
|
8807338 |
1996 |
rs75996173
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease.
|
9067749 |
1997 |
rs77316810
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease.
|
9067749 |
1997 |
rs79658334
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Oncogenic activation of RET by two distinct FMTC mutations affecting the tyrosine kinase domain.
|
9242375 |
1997 |
rs79658334
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinoma.
|
9398735 |
1997 |
rs79781594
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
RET in human development and oncogenesis.
|
9174404 |
1997 |
rs79890926
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinoma.
|
9068588 |
1997 |
rs79890926
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significance.
|
9146685 |
1997 |
rs75030001
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A.
|
9506724 |
1998 |
rs77939446
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Hirschsprung disease in MEN 2A: increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation.
|
9384613 |
1998 |
rs79658334
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A GTG to ATG novel point mutation at codon 804 in exon 14 of the RET proto-oncogene in two families affected by familial medullary thyroid carcinoma.
|
9452077 |
1998 |