|
| Entrez Id: |
5979 |
| Gene Symbol: |
RET |
RET
|
0.200 |
GeneticVariation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
23405 |
| Gene Symbol: |
DICER1 |
DICER1
|
0.120 |
GeneticVariation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
324 |
| Gene Symbol: |
APC |
APC
|
0.110 |
SusceptibilityMutation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
1019 |
| Gene Symbol: |
CDK4 |
CDK4
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
1495 |
| Gene Symbol: |
CTNNA1 |
CTNNA1
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
5965 |
| Gene Symbol: |
RECQL |
RECQL
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
5890 |
| Gene Symbol: |
RAD51B |
RAD51B
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
23164 |
| Gene Symbol: |
MPRIP |
MPRIP
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
6605 |
| Gene Symbol: |
SMARCE1 |
SMARCE1
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
3077 |
| Gene Symbol: |
HFE |
HFE
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
7516 |
| Gene Symbol: |
XRCC2 |
XRCC2
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
2132 |
| Gene Symbol: |
EXT2 |
EXT2
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
4913 |
| Gene Symbol: |
NTHL1 |
NTHL1
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
ABRAXAS1
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
4286 |
| Gene Symbol: |
MITF |
MITF
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
114034 |
| Gene Symbol: |
TOE1 |
TOE1
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
CDKN2B-AS1
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
201163 |
| Gene Symbol: |
FLCN |
FLCN
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
51023 |
| Gene Symbol: |
MRPS18C |
MRPS18C
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
2176 |
| Gene Symbol: |
FANCC |
FANCC
|
0.100 |
GeneticVariation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
5965 |
| Gene Symbol: |
RECQL |
RECQL
|
0.100 |
CausalMutation
|
group |
CLINVAR |
|
|
|
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
0.130 |
CausalMutation
|
group |
CLINVAR |
"""Second hit"" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivation."
|
11231323 |
2001 |
|
| Entrez Id: |
672 |
| Gene Symbol: |
BRCA1 |
BRCA1
|
0.150 |
CausalMutation
|
group |
CLINVAR |
"A new case of ""de novo"" BRCA1 mutation in a patient with early-onset breast cancer."
|
28265380 |
2017 |
|
| Entrez Id: |
7157 |
| Gene Symbol: |
TP53 |
TP53
|
0.170 |
CausalMutation
|
group |
CLINVAR |
"Apparently ""BRCA-related"" breast and ovarian cancer patient with germline TP53 mutation."
|
21535297 |
2011 |
|
| Entrez Id: |
5728 |
| Gene Symbol: |
PTEN |
PTEN
|
0.160 |
CausalMutation
|
group |
CLINVAR |
"Beta catenin and cytokine pathway dysregulation in patients with manifestations of the ""PTEN hamartoma tumor syndrome""."
|
22520842 |
2012 |