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 VCAN:
 
NM_001164098
Mutation details:
37
records
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10
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37
mutation records.
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4
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NM_004385
Mutation details:
69
records
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69
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7
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NM_001126336
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Mutation details:
18
records
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10
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18
mutation records.
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2
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NM_001164097
Mutation details:
50
records
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1
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10
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50
mutation records.
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5
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