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 PPRC1:
 
NM_001288727
Mutation details:
10
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NM_001288728
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Mutation details:
19
records
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1
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10
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19
mutation records.
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NM_015062
Mutation details:
19
records
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1
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10
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19
mutation records.
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