ESCCdb: An Integrated Database for Esophageal Squamous Cell Carcinoma
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Consensus DEGs
Recurrent Mutations
Significant CNV
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Somatic mutations of RHOH:
 
NM_001278359
Mutation details:
2
records
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NM_001278360
Mutation details:
2
records
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2
mutation records.
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NM_001278361
Mutation details:
2
records
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10
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2
mutation records.
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NM_001278362
Mutation details:
2
records
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2
mutation records.
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NM_001278363
Mutation details:
2
records
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1
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10
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2
mutation records.
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NM_001278364
Mutation details:
2
records
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1
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10
/
2
mutation records.
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NM_001278365
Mutation details:
2
records
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1
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10
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2
mutation records.
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NM_001278366
Mutation details:
2
records
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1
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10
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2
mutation records.
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NM_001278367
Mutation details:
2
records
Showing
1
-
10
/
2
mutation records.
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1
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1
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NM_001278368
Mutation details:
2
records
Showing
1
-
10
/
2
mutation records.
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1
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NM_001278369
Mutation details:
2
records
Showing
1
-
10
/
2
mutation records.
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1
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1
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NM_004310
Mutation details:
2
records
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1
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10
/
2
mutation records.
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