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 BCL11B:
 
NM_001282237
Mutation details:
9
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NM_138576
Mutation details:
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NM_001282238
Mutation details:
7
records
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7
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NM_022898
Mutation details:
7
records
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10
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7
mutation records.
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