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 PPP1R9A:
 
NM_001166160
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Mutation details:
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NM_001166161
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Mutation details:
45
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10
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45
mutation records.
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NM_001166162
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Mutation details:
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NM_001166163
Mutation details:
38
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NM_017650
Mutation details:
38
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