|
| Entrez Id: |
7048 |
| Gene Symbol: |
TGFBR2 |
TGFBR2
|
0.610 |
GeneticVariation
|
disease |
UNIPROT |
A dominant negative mutation of transforming growth factor-beta receptor type II gene in microsatellite stable oesophageal carcinoma.
|
10789724 |
2000 |
|
| Entrez Id: |
1630 |
| Gene Symbol: |
DCC |
DCC
|
0.500 |
GeneticVariation
|
disease |
UNIPROT |
|
|
|
|
| Entrez Id: |
49860 |
| Gene Symbol: |
CRNN |
CRNN
|
0.320 |
GeneticVariation
|
disease |
UNIPROT |
Genetic variants of C1orf10 and risk of esophageal squamous cell carcinoma in a Chinese population.
|
19558548 |
2009 |
|
| Entrez Id: |
7048 |
| Gene Symbol: |
TGFBR2 |
TGFBR2
|
0.610 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
51741 |
| Gene Symbol: |
WWOX |
WWOX
|
0.410 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
6049 |
| Gene Symbol: |
RNF6 |
RNF6
|
0.400 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
324 |
| Gene Symbol: |
APC |
APC
|
0.160 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
79651 |
| Gene Symbol: |
RHBDF2 |
RHBDF2
|
0.150 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
6772 |
| Gene Symbol: |
STAT1 |
STAT1
|
0.110 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
9940 |
| Gene Symbol: |
DLEC1 |
DLEC1
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
4481 |
| Gene Symbol: |
MSR1 |
MSR1
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
115908 |
| Gene Symbol: |
CTHRC1 |
CTHRC1
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
51008 |
| Gene Symbol: |
ASCC1 |
ASCC1
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
7048 |
| Gene Symbol: |
TGFBR2 |
TGFBR2
|
0.610 |
CausalMutation
|
disease |
CGI |
|
|
|
|
| Entrez Id: |
1630 |
| Gene Symbol: |
DCC |
DCC
|
0.500 |
CausalMutation
|
disease |
CGI |
|
|
|
|
| Entrez Id: |
1956 |
| Gene Symbol: |
EGFR |
EGFR
|
0.500 |
CausalMutation
|
disease |
CGI |
|
|
|
|
| Entrez Id: |
51741 |
| Gene Symbol: |
WWOX |
WWOX
|
0.410 |
CausalMutation
|
disease |
CGI |
|
|
|
|
| Entrez Id: |
6049 |
| Gene Symbol: |
RNF6 |
RNF6
|
0.400 |
CausalMutation
|
disease |
CGI |
|
|
|
|
| Entrez Id: |
11178 |
| Gene Symbol: |
LZTS1 |
LZTS1
|
0.300 |
CausalMutation
|
disease |
CGI |
|
|
|
|
| Entrez Id: |
1956 |
| Gene Symbol: |
EGFR |
EGFR
|
0.500 |
GeneticVariation
|
disease |
CLINVAR |
Gefitinib-sensitizing mutations in esophageal carcinoma.
|
16707764 |
2006 |
|
| Entrez Id: |
1956 |
| Gene Symbol: |
EGFR |
EGFR
|
0.500 |
GeneticVariation
|
disease |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
|
| Entrez Id: |
1499 |
| Gene Symbol: |
CTNNB1 |
CTNNB1
|
0.200 |
GeneticVariation
|
disease |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
|
| Entrez Id: |
1029 |
| Gene Symbol: |
CDKN2A |
CDKN2A
|
0.200 |
GeneticVariation
|
disease |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
|
| Entrez Id: |
5290 |
| Gene Symbol: |
PIK3CA |
PIK3CA
|
0.200 |
GeneticVariation
|
disease |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
|
| Entrez Id: |
7157 |
| Gene Symbol: |
TP53 |
TP53
|
0.200 |
GeneticVariation
|
disease |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |