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 FRS2:
 
NM_001042555
Mutation details:
8
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NM_001278351
Mutation details:
8
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NM_001278353
Mutation details:
8
records
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NM_001278354
Mutation details:
8
records
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1
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10
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8
mutation records.
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NM_001278355
Mutation details:
8
records
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1
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10
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8
mutation records.
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NM_001278356
Mutation details:
8
records
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1
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10
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8
mutation records.
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NM_001278357
Mutation details:
8
records
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1
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10
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8
mutation records.
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NM_006654
Mutation details:
8
records
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10
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8
mutation records.
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