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 AP2S1:
 
NM_001301076
Mutation details:
3
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NM_001301078
Mutation details:
3
records
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NM_001301081
Mutation details:
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NM_004069
Mutation details:
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NM_021575
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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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