rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers.
|
28503760 |
2018 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Mediastinal paragangliomas related to SDHx gene mutations.
|
27785149 |
2016 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytoma.
|
25371406 |
2015 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Phenotype of SDHB mutation carriers in the Netherlands.
|
25047027 |
2014 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Missense mutations in the human SDHB gene increase protein degradation without altering intrinsic enzymatic function.
|
22835832 |
2012 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Structural basis for malfunction in complex II.
|
22904323 |
2012 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.
|
22517554 |
2012 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
|
19454582 |
2009 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Germline SDHB mutations are common in patients with apparently sporadic sympathetic paragangliomas.
|
18382370 |
2008 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Clinical presentations, biochemical phenotypes, and genotype-phenotype correlations in patients with succinate dehydrogenase subunit B-associated pheochromocytomas and paragangliomas.
|
17200167 |
2007 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Germ-line mutations in nonsyndromic pheochromocytoma.
|
12000816 |
2002 |
rs786202732
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Effect of cysteine to serine mutations on the properties of the [4Fe-4S] center in Escherichia coli fumarate reductase.
|
7547971 |
1995 |