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 CNR1:
 
NM_001160226
Mutation details:
16
records
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10
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16
mutation records.
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NM_001160258
Mutation details:
16
records
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NM_001160259
Mutation details:
16
records
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10
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16
mutation records.
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NM_016083
Mutation details:
16
records
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10
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16
mutation records.
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NM_033181
Mutation details:
16
records
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1
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10
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16
mutation records.
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