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 PTPRD:
 
NM_002839
Mutation details:
67
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NM_001040712
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Mutation details:
58
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NM_001171025
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Mutation details:
57
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NM_130391
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Mutation details:
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NM_130392
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Mutation details:
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NM_130393
Mutation details:
57
records
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1
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10
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57
mutation records.
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6
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